CA2140598C - Prolineamide derivatives - Google Patents
Prolineamide derivatives Download PDFInfo
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- CA2140598C CA2140598C CA002140598A CA2140598A CA2140598C CA 2140598 C CA2140598 C CA 2140598C CA 002140598 A CA002140598 A CA 002140598A CA 2140598 A CA2140598 A CA 2140598A CA 2140598 C CA2140598 C CA 2140598C
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- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/0606—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing heteroatoms not provided for by C07K5/06086 - C07K5/06139, e.g. Ser, Met, Cys, Thr
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Abstract
The present invention is directed to a prolineamide derivative represented by the formula (I): (see formula I) or a salt or hydrate thereof or a pharmaceutically acceptable salt thereof, which has a protease inhibition activity and is useful as an active ingredient of pharmaceutical compositions.
Description
PROLINEAMIDE DERIVATIVES
FIELD OF THE INVENTION
The present invention relates to novel proline derivatives.
BACKGROUND OF THE INVENTION
It is known that various proteases are present in the living body, for example, a group of serine proteases such as thrombin, factor Xa, factor IXa, factor Vlla, trypsin, plasmin, tissue plasminogen activator, kallikrein, C3/C5 convertase in the complement system, tryptase, etc. is known. Further, it is also known that these proteases cause various diseases when they are activated abnormally. Accordingly, substances which inhibit the activity of these proteases may be useful as clinical remedies. For example, antithrombin agents, anti-factor Xa agents and anti-factor Vlla agents are useful for treating thrombosis, antitrypsin agents are useful for treating pancreatitis, antiplasmin agents are useful as hemostatics, antiallergic agents and antiinflammatory agents, antikallikrein agents are useful as a remedy for inflammation and ulcer, and anticomplementary agents are useful as a remedy for nephritis and rheumatoid arthritis. Protease inhibitors having these actions have hitherto been developed, but they are not sufficient for practical use in view of protease inhibition activity, stability in the living body etc. For ;~
example, tripeptide derivatives consisting of arginine derivatives are known as protease inhibitors. That is, D-phenylalanyl-L-prolyl-L-arginal is known as a thrombin inhibitor (e.g. Folia Haematol., 109, 22 (1982)) but the molecule is fairly unstable in the living body (J. Med. Chem., 33, 1729 (1990)). Further, arginal derivatives (Japanese Laid-open Patent Publication No. 4-89498) or arnidinophenylaianine derivatives (Thromb. Res., 17, 425 (1980)) are reported as protease inhibitors but their inhibition activity is low.
Under these circumstances, the present inventors have studied to develop structurally novel drugs having enzyme inhibition activity and stability in vivo, which are sufficient for practical use. As a result, it has been found that certain prolineamide derivatives can attain the desired object, thus the present invention has been established.
SUMMARY OF THE INVENTION
The present invention provides a prolineamide derivative represented by the formula (I):
tCH2) 0 I I
CNCH2 ~A-R3 N7~ i R2 --- (1) C=0 R' wherein A is a carbon atom or a nitrogen atom; n is an integer of 0 to 2; a broken line is absent or a single bond;
FIELD OF THE INVENTION
The present invention relates to novel proline derivatives.
BACKGROUND OF THE INVENTION
It is known that various proteases are present in the living body, for example, a group of serine proteases such as thrombin, factor Xa, factor IXa, factor Vlla, trypsin, plasmin, tissue plasminogen activator, kallikrein, C3/C5 convertase in the complement system, tryptase, etc. is known. Further, it is also known that these proteases cause various diseases when they are activated abnormally. Accordingly, substances which inhibit the activity of these proteases may be useful as clinical remedies. For example, antithrombin agents, anti-factor Xa agents and anti-factor Vlla agents are useful for treating thrombosis, antitrypsin agents are useful for treating pancreatitis, antiplasmin agents are useful as hemostatics, antiallergic agents and antiinflammatory agents, antikallikrein agents are useful as a remedy for inflammation and ulcer, and anticomplementary agents are useful as a remedy for nephritis and rheumatoid arthritis. Protease inhibitors having these actions have hitherto been developed, but they are not sufficient for practical use in view of protease inhibition activity, stability in the living body etc. For ;~
example, tripeptide derivatives consisting of arginine derivatives are known as protease inhibitors. That is, D-phenylalanyl-L-prolyl-L-arginal is known as a thrombin inhibitor (e.g. Folia Haematol., 109, 22 (1982)) but the molecule is fairly unstable in the living body (J. Med. Chem., 33, 1729 (1990)). Further, arginal derivatives (Japanese Laid-open Patent Publication No. 4-89498) or arnidinophenylaianine derivatives (Thromb. Res., 17, 425 (1980)) are reported as protease inhibitors but their inhibition activity is low.
Under these circumstances, the present inventors have studied to develop structurally novel drugs having enzyme inhibition activity and stability in vivo, which are sufficient for practical use. As a result, it has been found that certain prolineamide derivatives can attain the desired object, thus the present invention has been established.
SUMMARY OF THE INVENTION
The present invention provides a prolineamide derivative represented by the formula (I):
tCH2) 0 I I
CNCH2 ~A-R3 N7~ i R2 --- (1) C=0 R' wherein A is a carbon atom or a nitrogen atom; n is an integer of 0 to 2; a broken line is absent or a single bond;
y.
R1 is -D-(CH)n,-E-R4 f {wherein D and E independently indicate a single bond or an optionally branched C1-C6 alkylene group;
R4 is a Ci-C6 alkyl group, -OR6 (R6 is a hydrogen atom, a Ci-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted CTC12 aralkyl group), -SR7 (R7 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted CTC12 aralkyl group), -SOR8 (R8 is an optionally substituted C6-C10 aryl group or an optionally substituted C3-C$ cycloalkyl group), -S02R9 (R9 is an optionally substituted C6-C10 aryl group or an optionally substituted C3-C$
cycloalkyl group), -COR10 (RlO is a hydroxyl group, a Cl-CE; alkoxy group, an optionally substituted C6-C10 aryl group or an optionally substituted C3-C8 cycloalkyl group), -NHR1 1 (Rl 1 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted CTC12 aralkyl group), -NHCOR12 (R12 is a C1-C6 alkoxy group, an optionally substituted C6-C1o aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted CTC12 aralkyloxy group), -NHSO2R13 (R13 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group, ari optionally substituted CTC12 aralkyl group, an optionally substituted 5- to 10-membered heterocyclic group), an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group, an optionally substituted 5- to 10-membered heterocyclic group or -SiR14R15R16 (R14, R15, and R16 independently indicate a C1-C6 alkyl group);
R5 is a -OR17 (R17 is a hydrogen atom, -SiR22R23R24 (R22, R23, and R24 independently indicate a C1-C6 alkyl group), a C1-C6 alkyl group or an optionally substituted 5- to 10-membered heterocyclic group)), -OCOR18 (R18 is a hydrogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group, an amino group, a C1-C6 alkylamino group, a C2-C12 dialkylamino group or a C2-C7 alkenylamino group), -NHR19 (R19 is a hydrogen atom, a C1-C6 alkyl group or an optionally substituted CTC12 aralkyl group), -NHCOR20 (R20 is a hydrogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, an optionally substituted C3-C8 cycloalkyl group, a C2-C7 carboxyalkyloxy group, a C2-C7 alkenyloxy group, an optionally substituted C6-C10 aryl group, an optionally substituted C6-C10 aryloxy group, a C3-C9 alkoxycarbonylalkoxy group, a C2-C12 dialkylamino group or an optionally substituted CTC12 aralkyloxy group) or -NHSO2R21 (R21 is a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C2-C7 carboxyalkyl group, an optionally substituted C6-Clo aryl group, a C3-C9 alkoxycarbonylalkyl group or an optionally substituted C7-C12 aralkyl group);
andmis0or1};
R2 is a hydrogen atom or a Cl-C6 alkyl group; and R3 is -NH2 or -C(=NR25)NH2 (R25 is a hydrogen atom, or a hydroxyl group), provided that R3 is -C(=NRzS)NH2 when A is a nitrogen atom and further provided that when R4 and R5 are sulphonyl-amino, R3 is NH2, or a salt and pharmaceutical use thereof.
DETAILED DESCRIPTION OF THE INVENTION
The prolineamide derivative of the present invention is represented by the above formula (I). Examples of the optionally branched Cl-C6 alkylene group in the above definition include -CH2-, -(CH2)2-, -(CH2)3-, -(CH2)4-, -(CH2)5-, -(CH2)6-, -CH(CH3)-, -C(CH3)2-, -CH(CH3)CH2-, -CH2CH(CH3)-, -C(CH3)2CH2-, -CH2C(CH3)2-, -CH(CH3)CH(CH3)- and the like. Examples of the CI-C6 alkyl group include methyl group, ethyl group, n-propyl group, ipropyl group, n-butyl group, s--butyl group, i-butyl group, t-butyl group, n-pentyl group, n-hexyl group and the like. Examples of the C1-C3 alkyl group include 214'0598 those having three carbon atoms or less among those illustrated above.
Examples of the C1-C6 alkoxy group include methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butyloxy group, s-butyloxy group, i-butyloxy group, t-butyloxy group, n-pentyloxy group, n-hexyloxy group and the like.
Examples of the C2-C7 alkoxycarbonyl group include methoxycarbonyl group, ethoxycarbonyl group, n-propoxycarbonyl group, i-propoxyc:arbonyl group, n-butyloxycarbonyl group, t-butyloxycarbonyl group, n-pentyloxycarbonyl group, n-hexyloxycarbonyl group and the like. Examples of the C3-C8 cycloalkyl group include cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group and the like. Examples of the C6-C10 aryl group include phenyl group, tolyl group, naphthyl group and the like. Examples of the CTC12 aralkyl group include benzyl group, phenylethyl group, phenylpropyl group, naphthylmethyl group and the like.
Examples of the C6-C10 aryloxy group include phenyloxy group, naphthyloxy group and the like. Examples of the CTC12 aralkyloxy group include benzyloxy group, phenylethyloxy group, phenylpropyloxy group, naphthylmethyloxy group and the like. Examples of the heterocyclic group include those containing 1 to 4 heteroatoms selected from an oxygen atom, a sulfur atom and a nitrogen atom and the total number of atoms constituting the ring is 5 to 10, specifically, respective residues of furan ring, tetrahydrofuran ring, pyran ring, benzofuran ring, chroman ring, thiophene ring, benzothiophene ring, pyrrole ring, imidazole ring, pyrazole ring, triazole ring, pyridine ring, piperidine ring, pyrazine ring, piperazine ring, pyrimidine ring, ~~
indole ring, benzimidazole ring, purine ring, quinoline ring, phthalazine ring, quinazoline ring, cinnoline ring, oxazole ring, thiazole ring, morpholine ring and the like. Examples of the C1-C6 haloalkyl group include chloromethyl group, bromomethyl group, dichloromethyl group, 1-chloroethyl group, 2-chloroethyl group, 3-chloropropyl group, 4-chlorobutyl group, 5-chloropentyl group, 6-chlorohexyl group, difluoromethyl group, trifluoroniethyl group and the like. Examples of the C2-C7 carboxyalkyl group include carboxymethyl group, 2-carboxyethyl group, 3-carboxypropyl group, 4-carboxybutyl group, 5-carboxypentyl group, 6-carboxyhexyl group and the like. Examples of the C2-C7 carboxyalkyloxy group include carboxymethoxy group, 2-carboxyethoxy group, 3-carboxypropoxy group, 4-carboxybutyloxy group, 5-carboxypentyloxy group, 6-carboxyhexyloxy group and the like. Examples of the C2-C7 alkenyloxy group include vinyloxy group, aryloxy group, 2-propenyloxy group, isopropenyloxy group, 3-butenyloxy group, 4-pentenyloxy group, 5-hexenyloxy group and the like. Examples of the C2-C7 alkenylamino group include vinylamino group, arylamino group, 2-propenylamino group, isopropenylamino group, 3-butenylamino group, 4-pentenylamino group, 5-hexenylamino group and the like. Examples of the C1-C6 alkylamino group include methylamino group, ethylamino group, n-propylamino group, n-butylamino group and the like. Examples of the C2-C12 dialkylamino group include dimethylamino group, methylethylamino group, diethylamino group, di-n-propylamino group and the like. Examples of the C2-C7 acyl group include acetyl group, propionyl group, butyryl group, isobutyryl group, valeryl group, isovaleryl group, pivaroyl 2140598.
group, hexanoyl group, heptanoyl group and the like. Examples of the C2-C7 acyloxy group include acetyloxy group, propionyloxy group, butyryloxy group, isobutyryloxy group, valeryloxy group, isovaleryloxy group, pivaroyloxy group, hexanoyloxy group, heptanoyloxy group and the like. Examples of the C2-C7 alkoxycarbonyloxy group include methoxycarbonyloxy group, ethoxycarbonyloxy group, n-propoxycarbonyloxy group, n-butyloxycarbonyloxy group, n-pentyloxycarbonyloxy group, n-hexyloxycarbonyloxy group and the like. Examples of the C2-C7 hydroxyalkylcarbonyloxy group include hydroxymethylcarbonyloxy group, 2-hydroxyethylcarbonyloxy group, 3-hydroxypropylcarbonyloxy group, 4-hydroxybutyicarbonyloxy group, 5-hydroxypentylcarbonyloxy group, 6-hydroxyhexylcarbonyloxy group and the like. Examples of the C3-C9 alkoxycarbonylalkoxy group include methoxycarbonylmethoxy group, ethoxycarbonylmethoxy group, propoxycarbonylmethoxy group, methoxycarbonylethoxy group, ethoxycarbonylethoxy group, propoxycarbonylethoxy group and the like.
Examples of the C3-C9 alkoxycarbonylalkyl group include methoxycarbonylmethyl group, ethoxycarbonylmethyl group, propoxycarbonylmethyl group, methoxycarbonylethyl group, methoxycarbonylmethyl group, propoxycarbonylethyl group and the like.
Examples of the substituent in the above definition of "optionally substituted (with substituent)" include above-described C1-C6 alkyl group;
above-described C1-C6 haloalkyl group; above-described C1-C6 alkoxy group;
hydroxyl group; carboxyl group; above-described C2-C7 carboxyalkyl group;
R1 is -D-(CH)n,-E-R4 f {wherein D and E independently indicate a single bond or an optionally branched C1-C6 alkylene group;
R4 is a Ci-C6 alkyl group, -OR6 (R6 is a hydrogen atom, a Ci-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted CTC12 aralkyl group), -SR7 (R7 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted CTC12 aralkyl group), -SOR8 (R8 is an optionally substituted C6-C10 aryl group or an optionally substituted C3-C$ cycloalkyl group), -S02R9 (R9 is an optionally substituted C6-C10 aryl group or an optionally substituted C3-C$
cycloalkyl group), -COR10 (RlO is a hydroxyl group, a Cl-CE; alkoxy group, an optionally substituted C6-C10 aryl group or an optionally substituted C3-C8 cycloalkyl group), -NHR1 1 (Rl 1 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted CTC12 aralkyl group), -NHCOR12 (R12 is a C1-C6 alkoxy group, an optionally substituted C6-C1o aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted CTC12 aralkyloxy group), -NHSO2R13 (R13 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group, ari optionally substituted CTC12 aralkyl group, an optionally substituted 5- to 10-membered heterocyclic group), an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group, an optionally substituted 5- to 10-membered heterocyclic group or -SiR14R15R16 (R14, R15, and R16 independently indicate a C1-C6 alkyl group);
R5 is a -OR17 (R17 is a hydrogen atom, -SiR22R23R24 (R22, R23, and R24 independently indicate a C1-C6 alkyl group), a C1-C6 alkyl group or an optionally substituted 5- to 10-membered heterocyclic group)), -OCOR18 (R18 is a hydrogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group, an amino group, a C1-C6 alkylamino group, a C2-C12 dialkylamino group or a C2-C7 alkenylamino group), -NHR19 (R19 is a hydrogen atom, a C1-C6 alkyl group or an optionally substituted CTC12 aralkyl group), -NHCOR20 (R20 is a hydrogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, an optionally substituted C3-C8 cycloalkyl group, a C2-C7 carboxyalkyloxy group, a C2-C7 alkenyloxy group, an optionally substituted C6-C10 aryl group, an optionally substituted C6-C10 aryloxy group, a C3-C9 alkoxycarbonylalkoxy group, a C2-C12 dialkylamino group or an optionally substituted CTC12 aralkyloxy group) or -NHSO2R21 (R21 is a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C2-C7 carboxyalkyl group, an optionally substituted C6-Clo aryl group, a C3-C9 alkoxycarbonylalkyl group or an optionally substituted C7-C12 aralkyl group);
andmis0or1};
R2 is a hydrogen atom or a Cl-C6 alkyl group; and R3 is -NH2 or -C(=NR25)NH2 (R25 is a hydrogen atom, or a hydroxyl group), provided that R3 is -C(=NRzS)NH2 when A is a nitrogen atom and further provided that when R4 and R5 are sulphonyl-amino, R3 is NH2, or a salt and pharmaceutical use thereof.
DETAILED DESCRIPTION OF THE INVENTION
The prolineamide derivative of the present invention is represented by the above formula (I). Examples of the optionally branched Cl-C6 alkylene group in the above definition include -CH2-, -(CH2)2-, -(CH2)3-, -(CH2)4-, -(CH2)5-, -(CH2)6-, -CH(CH3)-, -C(CH3)2-, -CH(CH3)CH2-, -CH2CH(CH3)-, -C(CH3)2CH2-, -CH2C(CH3)2-, -CH(CH3)CH(CH3)- and the like. Examples of the CI-C6 alkyl group include methyl group, ethyl group, n-propyl group, ipropyl group, n-butyl group, s--butyl group, i-butyl group, t-butyl group, n-pentyl group, n-hexyl group and the like. Examples of the C1-C3 alkyl group include 214'0598 those having three carbon atoms or less among those illustrated above.
Examples of the C1-C6 alkoxy group include methoxy group, ethoxy group, n-propoxy group, i-propoxy group, n-butyloxy group, s-butyloxy group, i-butyloxy group, t-butyloxy group, n-pentyloxy group, n-hexyloxy group and the like.
Examples of the C2-C7 alkoxycarbonyl group include methoxycarbonyl group, ethoxycarbonyl group, n-propoxycarbonyl group, i-propoxyc:arbonyl group, n-butyloxycarbonyl group, t-butyloxycarbonyl group, n-pentyloxycarbonyl group, n-hexyloxycarbonyl group and the like. Examples of the C3-C8 cycloalkyl group include cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group and the like. Examples of the C6-C10 aryl group include phenyl group, tolyl group, naphthyl group and the like. Examples of the CTC12 aralkyl group include benzyl group, phenylethyl group, phenylpropyl group, naphthylmethyl group and the like.
Examples of the C6-C10 aryloxy group include phenyloxy group, naphthyloxy group and the like. Examples of the CTC12 aralkyloxy group include benzyloxy group, phenylethyloxy group, phenylpropyloxy group, naphthylmethyloxy group and the like. Examples of the heterocyclic group include those containing 1 to 4 heteroatoms selected from an oxygen atom, a sulfur atom and a nitrogen atom and the total number of atoms constituting the ring is 5 to 10, specifically, respective residues of furan ring, tetrahydrofuran ring, pyran ring, benzofuran ring, chroman ring, thiophene ring, benzothiophene ring, pyrrole ring, imidazole ring, pyrazole ring, triazole ring, pyridine ring, piperidine ring, pyrazine ring, piperazine ring, pyrimidine ring, ~~
indole ring, benzimidazole ring, purine ring, quinoline ring, phthalazine ring, quinazoline ring, cinnoline ring, oxazole ring, thiazole ring, morpholine ring and the like. Examples of the C1-C6 haloalkyl group include chloromethyl group, bromomethyl group, dichloromethyl group, 1-chloroethyl group, 2-chloroethyl group, 3-chloropropyl group, 4-chlorobutyl group, 5-chloropentyl group, 6-chlorohexyl group, difluoromethyl group, trifluoroniethyl group and the like. Examples of the C2-C7 carboxyalkyl group include carboxymethyl group, 2-carboxyethyl group, 3-carboxypropyl group, 4-carboxybutyl group, 5-carboxypentyl group, 6-carboxyhexyl group and the like. Examples of the C2-C7 carboxyalkyloxy group include carboxymethoxy group, 2-carboxyethoxy group, 3-carboxypropoxy group, 4-carboxybutyloxy group, 5-carboxypentyloxy group, 6-carboxyhexyloxy group and the like. Examples of the C2-C7 alkenyloxy group include vinyloxy group, aryloxy group, 2-propenyloxy group, isopropenyloxy group, 3-butenyloxy group, 4-pentenyloxy group, 5-hexenyloxy group and the like. Examples of the C2-C7 alkenylamino group include vinylamino group, arylamino group, 2-propenylamino group, isopropenylamino group, 3-butenylamino group, 4-pentenylamino group, 5-hexenylamino group and the like. Examples of the C1-C6 alkylamino group include methylamino group, ethylamino group, n-propylamino group, n-butylamino group and the like. Examples of the C2-C12 dialkylamino group include dimethylamino group, methylethylamino group, diethylamino group, di-n-propylamino group and the like. Examples of the C2-C7 acyl group include acetyl group, propionyl group, butyryl group, isobutyryl group, valeryl group, isovaleryl group, pivaroyl 2140598.
group, hexanoyl group, heptanoyl group and the like. Examples of the C2-C7 acyloxy group include acetyloxy group, propionyloxy group, butyryloxy group, isobutyryloxy group, valeryloxy group, isovaleryloxy group, pivaroyloxy group, hexanoyloxy group, heptanoyloxy group and the like. Examples of the C2-C7 alkoxycarbonyloxy group include methoxycarbonyloxy group, ethoxycarbonyloxy group, n-propoxycarbonyloxy group, n-butyloxycarbonyloxy group, n-pentyloxycarbonyloxy group, n-hexyloxycarbonyloxy group and the like. Examples of the C2-C7 hydroxyalkylcarbonyloxy group include hydroxymethylcarbonyloxy group, 2-hydroxyethylcarbonyloxy group, 3-hydroxypropylcarbonyloxy group, 4-hydroxybutyicarbonyloxy group, 5-hydroxypentylcarbonyloxy group, 6-hydroxyhexylcarbonyloxy group and the like. Examples of the C3-C9 alkoxycarbonylalkoxy group include methoxycarbonylmethoxy group, ethoxycarbonylmethoxy group, propoxycarbonylmethoxy group, methoxycarbonylethoxy group, ethoxycarbonylethoxy group, propoxycarbonylethoxy group and the like.
Examples of the C3-C9 alkoxycarbonylalkyl group include methoxycarbonylmethyl group, ethoxycarbonylmethyl group, propoxycarbonylmethyl group, methoxycarbonylethyl group, methoxycarbonylmethyl group, propoxycarbonylethyl group and the like.
Examples of the substituent in the above definition of "optionally substituted (with substituent)" include above-described C1-C6 alkyl group;
above-described C1-C6 haloalkyl group; above-described C1-C6 alkoxy group;
hydroxyl group; carboxyl group; above-described C2-C7 carboxyalkyl group;
214 0- 59 8 ~.
above-described C2-C7 carboxyalkyloxy group; above-described C2-C7 acyl group; above-described C2-C7 acyloxy group; above-described C2-C7 alkoxycarbonyl group; above-described C2-C7 alkoxycarbonyloxy group; C8-C13 aralkyloxycarbonyl group such as benzyloxycarbonyl group, phenylethyloxycarbonyl group, phenyipropyloxycarbonyl group, riaphthylmethyloxycarbonyl group, etc.; halogen atoms such as fluorine atom, chlorine atom, bromine atom and the like.
In the compound represented by the above formula (I), it is preferred that the 5- to 10-membered heterocyclic group contains 1 to 4 heteroatoms selected from the group consisting of an oxygen atom, a sulfur atom and a nitrogen atom and the total number of atoms constituting the ring is 5 to 10. Further, as the substituent of the respective groups, a group(s) selected from C1-C6 alkyl group, C1-C6 haloalkyl group, C1-C6 alkoxy group, hydroxyl group, carboxyl group, C2-carboxyalkyl group, C2-C7 carboxyalkyloxy group, C2-C7 acyl group, C2-C7 acyloxy group, C2-C7 alkoxycarbonyl group, C2-C7 alkoxycarbonyloxy group, C8-C13 aralkyloxycarbonyl group, C3-C9 alkoxycarbonylalkoxy group and halogen atoms is preferred.
In the compound represented by the above formula (I) of the present invention, a carbon atom is preferred as A.
Examples of preferred compounds of the present invention include those of the formula (I), wherein A is a carbon atom; n is 1 or 2; R1 is .:, -D-(CH)m-E-R4 {wherein D and E independently indicate a single bond or an optionally branched Ci -C6 alkylene group;
R4 is a C1-C6 alkyl group: -OR6 (R6 is a C1-C6 alkyl group; a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a Ci-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a Cs-Cg alkoxycarbonylalkoxy group and a benzyloxycarbonyl group; or a CTC12 aralkyl group which rnay be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group): -SR7 (R7 is a Ci-C6 alkyl group, a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group; or a CTC12 aralkyl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a ("2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group): -COOH: a C6-C1o aryl group which may be substituted with at least one substituent selected from the group consisting of a Ci-C6 alkyl group, a Cl-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-Cg alkoxycarbonylalkoxy group and a benzyloxycarbonyl group: a C3-C8 cycloalkyl group: or -SiR14R15R16 (R14, R15, and R16 independently indicate a Ci -C6 alkyl group);
R5 is -OH, -OCOR18 (R18 is a C1-C6 alkoxy group or a C2-C7 alkenylamino group), -NH2, -NHCOR20 (R20 is a C1-C6 alkoxy group, a C6-C10 aryloxy group, a C3-C9 alkoxycarbonylalkoxy group, a C2-C;12 dialkylamino group or a CTC12 aralkyloxy group) or -NHSO2R21 (R21 is a C1-C6 alkyl group, a C2-C7 carboxyalkyl group, a C6-C10 aryl group, a ('3-C9 alkoxycarbonylalkyl group or a CTC12 aralkyl group);
above-described C2-C7 carboxyalkyloxy group; above-described C2-C7 acyl group; above-described C2-C7 acyloxy group; above-described C2-C7 alkoxycarbonyl group; above-described C2-C7 alkoxycarbonyloxy group; C8-C13 aralkyloxycarbonyl group such as benzyloxycarbonyl group, phenylethyloxycarbonyl group, phenyipropyloxycarbonyl group, riaphthylmethyloxycarbonyl group, etc.; halogen atoms such as fluorine atom, chlorine atom, bromine atom and the like.
In the compound represented by the above formula (I), it is preferred that the 5- to 10-membered heterocyclic group contains 1 to 4 heteroatoms selected from the group consisting of an oxygen atom, a sulfur atom and a nitrogen atom and the total number of atoms constituting the ring is 5 to 10. Further, as the substituent of the respective groups, a group(s) selected from C1-C6 alkyl group, C1-C6 haloalkyl group, C1-C6 alkoxy group, hydroxyl group, carboxyl group, C2-carboxyalkyl group, C2-C7 carboxyalkyloxy group, C2-C7 acyl group, C2-C7 acyloxy group, C2-C7 alkoxycarbonyl group, C2-C7 alkoxycarbonyloxy group, C8-C13 aralkyloxycarbonyl group, C3-C9 alkoxycarbonylalkoxy group and halogen atoms is preferred.
In the compound represented by the above formula (I) of the present invention, a carbon atom is preferred as A.
Examples of preferred compounds of the present invention include those of the formula (I), wherein A is a carbon atom; n is 1 or 2; R1 is .:, -D-(CH)m-E-R4 {wherein D and E independently indicate a single bond or an optionally branched Ci -C6 alkylene group;
R4 is a C1-C6 alkyl group: -OR6 (R6 is a C1-C6 alkyl group; a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a Ci-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a Cs-Cg alkoxycarbonylalkoxy group and a benzyloxycarbonyl group; or a CTC12 aralkyl group which rnay be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group): -SR7 (R7 is a Ci-C6 alkyl group, a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group; or a CTC12 aralkyl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a ("2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group): -COOH: a C6-C1o aryl group which may be substituted with at least one substituent selected from the group consisting of a Ci-C6 alkyl group, a Cl-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-Cg alkoxycarbonylalkoxy group and a benzyloxycarbonyl group: a C3-C8 cycloalkyl group: or -SiR14R15R16 (R14, R15, and R16 independently indicate a Ci -C6 alkyl group);
R5 is -OH, -OCOR18 (R18 is a C1-C6 alkoxy group or a C2-C7 alkenylamino group), -NH2, -NHCOR20 (R20 is a C1-C6 alkoxy group, a C6-C10 aryloxy group, a C3-C9 alkoxycarbonylalkoxy group, a C2-C;12 dialkylamino group or a CTC12 aralkyloxy group) or -NHSO2R21 (R21 is a C1-C6 alkyl group, a C2-C7 carboxyalkyl group, a C6-C10 aryl group, a ('3-C9 alkoxycarbonylalkyl group or a CTC12 aralkyl group);
214a59s and m is 0 or 11;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2 (R25 is a hydrogen atom, a C2-C7 alkoxycarbonyl group or a hydroxyl group), -NH-C(=NR25)NH2 (R25 is as defined above) or -NHR26 (R26 is a hydrogen atom, a C2-C7 alkoxycarbonyl group or a 5-C1-C3 alkyl-1,3-dioxol-2-on-4-ylmethyl group).
As the more preferred compound of the present invention, there is a compound of the formula (I), wherein A is a carbon atom; n is 1; Rl is -D-(CH)m-E-R4 I
(wherein D and E independently indicate a single bond or an optionally branched C1-C6 alkylene group;
R4 is a C1-C6 alkyl group; -OR6 (R6 is a C6-C10 aryl or CTC12 aralkyl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group); -SR7 (R7 is a C1-C6 alkyl group); a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a Cl-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group; or a C3-C6 cycloalkyl group;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2 (R25 is a hydrogen atom, a C2-C7 alkoxycarbonyl group or a hydroxyl group), -NH-C(=NR25)NH2 (R25 is as defined above) or -NHR26 (R26 is a hydrogen atom, a C2-C7 alkoxycarbonyl group or a 5-C1-C3 alkyl-1,3-dioxol-2-on-4-ylmethyl group).
As the more preferred compound of the present invention, there is a compound of the formula (I), wherein A is a carbon atom; n is 1; Rl is -D-(CH)m-E-R4 I
(wherein D and E independently indicate a single bond or an optionally branched C1-C6 alkylene group;
R4 is a C1-C6 alkyl group; -OR6 (R6 is a C6-C10 aryl or CTC12 aralkyl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group); -SR7 (R7 is a C1-C6 alkyl group); a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a Cl-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group; or a C3-C6 cycloalkyl group;
R5 is -OH, -NH2, -NHCOR20 (R20 is a C1-C6 alkoxy group or a CTC12 aralkyloxy group) or -NHSO2R21 (R21 is a C1-C6 alkyl group or a C6-C10 aryl group);
and m is 1 };
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2 (R25 is a hydrogen atom or a hydroxyl group) or -NH2.
As the more preferred compound of the present invention, there is a compound of the formula (I), wherein A is a carbon atom; n is 1; R1 is -D-(CH)m-E-R4 I
{wherein D is a single bond and E is a single bond or a C1-C6 alkylene group;
R4 is a Cl-C6 alkyl group; -OR6 (R6 is a C6-C10 aryl or CTC12 aralkyl group which may be substituted with at least one substituent selected from the group consisting of a Cl-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group); -SR7 (R7 is a Ci-C6 alkyl group); a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group; or a C3-C6 cycloalkyl group;
and m is 1 };
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2 (R25 is a hydrogen atom or a hydroxyl group) or -NH2.
As the more preferred compound of the present invention, there is a compound of the formula (I), wherein A is a carbon atom; n is 1; R1 is -D-(CH)m-E-R4 I
{wherein D is a single bond and E is a single bond or a C1-C6 alkylene group;
R4 is a Cl-C6 alkyl group; -OR6 (R6 is a C6-C10 aryl or CTC12 aralkyl group which may be substituted with at least one substituent selected from the group consisting of a Cl-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group); -SR7 (R7 is a Ci-C6 alkyl group); a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group; or a C3-C6 cycloalkyl group;
2 14 A5 9 8 :
R5 is -NH2, -NHCOR20 (R20 is a Cl-C6 alkoxy group or a CTC12 aralkyloxy group) or -NHSO2R21 (R21 is a C1-C6 alkyl group or a C6-C1o aryl group);
and m is 1 };
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2 (R25 is a hydrogen atom or a hydroxyl group) or -NH2.
As the still more preferred compound of the present invention, there is a compound of the formula (I), wherein A is a carbon atom; n is 1; R1 is -D-(CH)m-E-R4 i {wherein D is a single bond; E is a single bond or a C1-C3 alkylene group; R4 is a C3-C6 alkyl group, -OR6 (R6 is a Cl-C6 alkyl group), a phenyl group or a C3-C6 cycloalkyl group; R5 is -OH, -NHR19 (R19 is a hydrogen atom), -NHCOR20 (R20 is a Cy-Cg alkoxy group) or -NHSO2R21 (R21 is a C1-C3 alkyl group); and m is 1};
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2 (R25 is a hydrogen atom or a hydroxyl group) or -NH2.
As the particularly preferred compound of the present invention, there is a compound of the formula (I), wherein A is a carbon atom; n is 1; R1 is -D-(CH)m-E-R4 I
{wherein D is a single bond; E is a single bond or a Cl-C6 alkylene group;
R4 is a C1-C6 alkyl group; R5 is -NHCOR20 (R20 is a C1-C6 alkoxy group); and m is 1 };
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2 (R25 is a hydrogen atom or a hydroxyl group).
As the most preferred compound of the present inverition, there is trans-4-[(S)-N-((R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 461 in Table 1 in Example 33).
The prolineamide derivatives represented by the above formula (I) can afford various stereoisomers. For example, concerning asymmetric carbon atoms, the absolute configuration may be D-configuration, L-configuration or DL configuration and all types thereof are included in the compounds of the present invention.
Examples of the salt which can be formed with the compounds of the above formula (I) of the present invention include inorganic acid salts such as hydrochloride, hydrobromide, hydroiodide, sulfate, nitrate, phosphate, etc.;
organic acid salts such as succinate, oxalate, fumarate, maleate, lactate, tartrate, citrate, acetate, glycolate, methanesulfonate, toluenesulfonate, etc.
R5 is -NH2, -NHCOR20 (R20 is a Cl-C6 alkoxy group or a CTC12 aralkyloxy group) or -NHSO2R21 (R21 is a C1-C6 alkyl group or a C6-C1o aryl group);
and m is 1 };
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2 (R25 is a hydrogen atom or a hydroxyl group) or -NH2.
As the still more preferred compound of the present invention, there is a compound of the formula (I), wherein A is a carbon atom; n is 1; R1 is -D-(CH)m-E-R4 i {wherein D is a single bond; E is a single bond or a C1-C3 alkylene group; R4 is a C3-C6 alkyl group, -OR6 (R6 is a Cl-C6 alkyl group), a phenyl group or a C3-C6 cycloalkyl group; R5 is -OH, -NHR19 (R19 is a hydrogen atom), -NHCOR20 (R20 is a Cy-Cg alkoxy group) or -NHSO2R21 (R21 is a C1-C3 alkyl group); and m is 1};
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2 (R25 is a hydrogen atom or a hydroxyl group) or -NH2.
As the particularly preferred compound of the present invention, there is a compound of the formula (I), wherein A is a carbon atom; n is 1; R1 is -D-(CH)m-E-R4 I
{wherein D is a single bond; E is a single bond or a Cl-C6 alkylene group;
R4 is a C1-C6 alkyl group; R5 is -NHCOR20 (R20 is a C1-C6 alkoxy group); and m is 1 };
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2 (R25 is a hydrogen atom or a hydroxyl group).
As the most preferred compound of the present inverition, there is trans-4-[(S)-N-((R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 461 in Table 1 in Example 33).
The prolineamide derivatives represented by the above formula (I) can afford various stereoisomers. For example, concerning asymmetric carbon atoms, the absolute configuration may be D-configuration, L-configuration or DL configuration and all types thereof are included in the compounds of the present invention.
Examples of the salt which can be formed with the compounds of the above formula (I) of the present invention include inorganic acid salts such as hydrochloride, hydrobromide, hydroiodide, sulfate, nitrate, phosphate, etc.;
organic acid salts such as succinate, oxalate, fumarate, maleate, lactate, tartrate, citrate, acetate, glycolate, methanesulfonate, toluenesulfonate, etc.
~~.
Further, the proline derivatives of the above formula (I) containing a free carboxyl group can also form a salt with a pharmaceutically acceptable base.
Examples of the salt include alkaline metal salt, alkaline earth metal salt, ammonium salt, alkyl ammonium salt and the like.
Further, the prolineamide derivatives of the above formula (I) and the salts thereof can also form a hydrate.
Hereinafter, examples of the compounds of the present invention will be described.
Further, the proline derivatives of the above formula (I) containing a free carboxyl group can also form a salt with a pharmaceutically acceptable base.
Examples of the salt include alkaline metal salt, alkaline earth metal salt, ammonium salt, alkyl ammonium salt and the like.
Further, the prolineamide derivatives of the above formula (I) and the salts thereof can also form a hydrate.
Hereinafter, examples of the compounds of the present invention will be described.
Table 1 (CH2) O
1 1 f9AR3 CNCH2 I C=0 I
R
Compound -(D(?H)mER4) ---No. -R1 -R2 -R3 F A B
roken line NH
1 -CH24~\~ -H _C// 1 C Single bond \ NH2 NH
2 -(CH2)24~ -H -C// 1 C Single bond NH
3 -(CH2)3 -H -C// 1 C Single bond 4 4 -(CH2)5-~, -H -C1 C Single bond NH
7----(CH2)8 -C 1 C Single bond 6 -(CH2)2 C~ -H // NH
C 1 C Single bond 7 -(CH2)2 -H -C// 1 C Single bond ~
8 -H -C 1 C Single bond -(CH2)2 Table 1 (continued) Compound R1 (-D-(cH)m-E-R4) -R2 -R3 n A Broken line NH
9 -(CH2)2 CH3 -H -C1 C Single bond \NH2 -(CH2)2 -H -C// 1 C Single bond ~
\NH2 OCHg NH
11 (CH2)2 -H -C// 1 C Single bond -~
\NH2 NH
12 -(CH2)2 //_~ OCH3 -H -C// 1 C Single bond \NH2 CI NH
13 -H -C 1 C Single bond -(CH2)2 \NH2 - -- --~
CI NH
-H -C 1 C Single bond 14 -(CH2)2 ~
- --~ N H
-(CH2)2 ~-\ -CI -H -C 1 C Single bond 16 -H 1 C Sin le bond -(CH2)2 C g - -- ~-- -;--F NH
17 -H -C 1 C Single bond -(CH2 )2 _2140598 Table 1 (continued) Compound -D-(CH)m-E-R4 No. -R1 I 5 -R2 -R3 n A Broken line R
NH
18 -(CH2)2 ~\\-F -H _C// 1 C Single bond 19 -H _C 1 C Single bond (CH2)2 - NH
1 1 f9AR3 CNCH2 I C=0 I
R
Compound -(D(?H)mER4) ---No. -R1 -R2 -R3 F A B
roken line NH
1 -CH24~\~ -H _C// 1 C Single bond \ NH2 NH
2 -(CH2)24~ -H -C// 1 C Single bond NH
3 -(CH2)3 -H -C// 1 C Single bond 4 4 -(CH2)5-~, -H -C1 C Single bond NH
7----(CH2)8 -C 1 C Single bond 6 -(CH2)2 C~ -H // NH
C 1 C Single bond 7 -(CH2)2 -H -C// 1 C Single bond ~
8 -H -C 1 C Single bond -(CH2)2 Table 1 (continued) Compound R1 (-D-(cH)m-E-R4) -R2 -R3 n A Broken line NH
9 -(CH2)2 CH3 -H -C1 C Single bond \NH2 -(CH2)2 -H -C// 1 C Single bond ~
\NH2 OCHg NH
11 (CH2)2 -H -C// 1 C Single bond -~
\NH2 NH
12 -(CH2)2 //_~ OCH3 -H -C// 1 C Single bond \NH2 CI NH
13 -H -C 1 C Single bond -(CH2)2 \NH2 - -- --~
CI NH
-H -C 1 C Single bond 14 -(CH2)2 ~
- --~ N H
-(CH2)2 ~-\ -CI -H -C 1 C Single bond 16 -H 1 C Sin le bond -(CH2)2 C g - -- ~-- -;--F NH
17 -H -C 1 C Single bond -(CH2 )2 _2140598 Table 1 (continued) Compound -D-(CH)m-E-R4 No. -R1 I 5 -R2 -R3 n A Broken line R
NH
18 -(CH2)2 ~\\-F -H _C// 1 C Single bond 19 -H _C 1 C Single bond (CH2)2 - NH
20 -(CH2)2 -H -C// 1 C Single bond --~ \
NH
NH
21 -(CH2)2 4_~\CF3 -H -C1 C Single bond OH NH
22 -(CH2)2 --H -C// 1 C Single bond NH
23 -(CH2)2 OH -H _C 1 C Single bond ~
NH
NH
24 -(CH2)2 (\ OH -H C1 C Single bond \NH2 COOH NH
25 ~~ -H _C// 1 C Single bond (CH2)2 \
COOH NH
COOH NH
26 -(CH2) -H _C// 1 C Single bond Table 1 (continued) Compound -(D(CH)mER4) ---No. -R~ -R2 -R3 n A Broken line .
R
NH
R
NH
27 -(CH2)2 COOH -H C// 1 C Single bond \NH2 NH
28 -(CH2)2 //\\ CH2COOH -H -C// 1 C Single bond \NH2 NH
29 -(CH2)2 // OCH2COOH -H _C 1 C Single bond \NH2 NH
30 -(CH2)2 \\ COOCH3 -H _C 1 C Single bond - --- -NH
31 -(CH2)2 //\ COOCH2 C -H C 1 C Single bond \
NH
NH
32 -(CH2)2 COCH3 -H _C 1 C Single bond \NH2 33 33 -CH2~ -H _C// 1 C Single bond \J \NH2 j -~
NH
NH
34 (CH2)2 __~ -H -C~~ 1 C Single bond ~ NH2 -- --~- -CHg NH
35 yCH3 -H C~~ 1 C Single bond (CH2)2 -H
- - -- -NH
- - -- -NH
36 (CH2)2 ~~
- H C1 C Single bond _21405g8 Table 1 (continued) Compound R~ (D(OH)mER4) -R2 -Rs n A Broken line No. R5 NH
- H C1 C Single bond _21405g8 Table 1 (continued) Compound R~ (D(OH)mER4) -R2 -Rs n A Broken line No. R5 NH
37 _(CH2)2 41 -H _C// 1 C Single bond NH
38 -(CH2)2 ~ N` -H _C 1 C Single bond NH
39 -(CH2)2 -NN-CH3 -H _C1 C Single bond \NH2 NH
40 H _C ~~ 1 C Single bond -(CH2)2 ~ -~,NH \NH2 NH
41 -CH3 -H C 1 C Single bond \NH2 NH
42 -CH2CH3 -H _C 1 C Single bond \NH2 NH
43 -(CH2)2CH3 -H _C// 1 C Single bond \NH2 NH
44 -CH(CH3)2 -H C// 1 C Single bond \NH2 -- --- --'-------- -NH
45 -(CH2)3CH3 -H C 1 C Single bond -- --- N M 46 -C(CH3)3 -H C~~ C Single bond Table 1 (continued) Compound -R1 (D(GH)mER4) -R2 -R3 n A Broken line NH
47 -(CH2)4CH3 -H C 1 C Single bond \NH2 NH
48 -CH2CH2C (CH3)3 -H -C// 1 C Single bond \NH2 NH
49 -(CH2)9CH3 -H -C/~ 1 C Single bond \NH2 NH
50 -CH2Si(CH3)3 -H _C 1 C Single bond \NH2 NH
51 -CH2CH2Si(CH3)3 -H -C// 1 C Single bond \NH2 NH 52 -CH2OCH3 -H -C// 1 C Single bond \NH2 NH
53 CH2O ~-H _C// 1 C Single bond \NH2 NH
54 -CH2O--~ -H _C// 1 C Single bond `-/ \NH2 NH
55 -CH2OCH2 - -H -C// 1 C Single bond \NH2 NH
56 -CH2OH -H _C// 1 C Single bond \NH2 NH
57 -CH2SCH3 -H -C// 1 C Single bond \NH2 _.
21.40598 Table 1 (continued) Compound -R1 D-(CH)m-E=R4 -R2 -R3 n A Broken line NH
58 -CH2S r\ -H -C 1 C Single bond \NH2 NH
59 -CH2S -H -C// 1 C Single bond \NH2 NH
60 -CH2SCH2 - C~ -H -C// 1 C Single bond \NH2 NH
61 -CH2SO-r) -H -C// 1 C Single bond \NH2 NH
62 -CH2SO--O -H -C 1 C Single bond \NH2 NH
63 -CH2SO2-H -C// 1 C Single bond \NH2 NH
64 -CH2SO2H> -H -C 1 C Single bond \NH2 NH
65 -CH2CO {~ `> -H -C 1 C Single bond ~--~ \NH2 NH
66 -CH2CO-O -H -C// 1 C Single bond \NH2 NH
67 -CH2COOH -H -C// 1 C Single bond \NH2 NH
68 -CH2COOCH3 -H -C// 1 C Single bond \NH2 Table 1 (continued) Comvpoound R-1 (-D-(cH)m-E-R4) _R2 -R3 n A Broken line NH
69 -CH2NHCH3 -H _C// 1 C Single bond \NH2 NH
70 -CH2NH ~~\ -H C 1 C Single bond \NH2 NH
71 -CH2NH-H) -H _C// 1 C Single bond ~ \NH2 NH
72 -CH2NHCH2 -C~ -H _C// 1 C Single bond \NH2 NH
73 -CH2NHCOOCH3 -H _C// 1 C Single bond \NH2 NH
74 CH2NHCO /-H C// 1 C Single bond \NH2 NH
75 -CH2NHCO-<~H) -H C// 1 C Single bond \NH2 NH
76 -CH2NHCOOCH2 -H _C 1 C Single bond -~
NH
77 -CH2NHSO2 - L~ -H -C 1 C Single bond S
- NH
78 -CH2NHSO2CH3 -H C 1 C Single bond -'-- -- - - -NH
79 -CH2NHSO2 -{~ -H _C 1 C Single bond Table 1 (continued) Compound (-D-(cH)m-E-R4) -R2 -R3 o -R1 n A Broken line NH
80 -CH2NHSO2CH2 -H _C// 1 C Single bond \NH2 NH
81 -CH2NHSO2 {H~ -H -C// 1 C Single bond \NH2 -(- NH
82 -CH-O -H -C// 1 C Single bond OH \NH2 -CHCH2C(CH3)g // NH
83 I -H _C 1 C Single bond OH \NH2 NH
84 -CH -H G// 1 C Single bond OSi(CH3)3 \NH2 ---- ----- -~--CHCH2C(CH3)3 NH
85 I -H _G 1 C Single bond O-CH3 \NH2 - -~-- --CHCH2C(CH3)3 NH
86 O/-~ -H 1 C Single bond O \NH2 _T -NH
87 -CH ~~ -H -C//
1 C Single bond NH
88 -H C// 1 C Single bond OCOCH3 \NH2 21~0598 Table 1 (continued) Compound R-1 (D(CH)mER4) -R2 -R3 I A Broken line -CHCH2C(CH3)3 /NH
89 I -H -C ~ 1 C Single bond OCOOCH3 \NH2 NH
90 -~H~ -H C// 1 C Single bond OCONH2 \NH2 NH
91 -CH /_ -H C// 1 C Single bond -CHCH2C(CH3)3 /NH
92 I -H -C ~ 1 C Single bond OCON(CH3)2 \NH2 93 -CH2CH-CH~ / NH
-H C 1 C Single bond OCONHCH2CH=CH2 NH2 NH
94 -CHCH2~ ~ ~ TH _C 1 C Single bond NHCHO \NH2 - ---~---I- - NH -CHCH2C(CH3)3 95 I -H C 1 C Single bond NHCOCH3 \NH
~ NH
96 CHCH2-< H;> -H C 1 C Single bond NHCOCF3~--~ \NH2 -- ---,--.--- -97 CHCH2 H _C// NH
1 C Single bond NHCOOCH3 \NH2 _ ,._ Table 1 (continued) Compound Ri (-D-(CH)m-E-R4'\ _R2 -R3 n A Broken line No. R5 CHC(SCH3)(CH3)2 // NH
98 -H C 1 C Single bond NHCOOC2H5 \NH2 NH
99 -CH H -H C1 C Single bond NHCO-C~ NH2 2 ~ ~ NH
100 -CH CH -H C1 C Single bond NHCO-<~ NH2 -CHCH2C(CH3)3 NH
101 I ~~ -H -C~~ 1 C Single bond \NH2 NH
102 -CHCH2 -H C 1 C Single bond NHCOOCH2CH=CH2 ~NH2 NH
103 -CHCH2 (\ COOH -H C// 1 C Single bond -CHCH2C(CH3)3 /NH
104 ~ -H -C ~ 1 C Single bond NH
105 ~H -H 1 C Single bond C
NHSO2CH3 \NHz __ Table 1 (continued) Compoound R' (DH)m.ER4) -R2 -R3 n A Broken line NH
106 -CHCH2- C -H C1 C Single bond NH
107 -CH /~\ -H _C1 C Single bond NHSO2CH3 ~NH2 NH
108 -CHCH2 () -H C 1 C Single bond NHSO2CH3 ~NH2 NH
-CH(CH2)3CH3 109 1 -H _C 1 C Single bond NHSO2CH3 \NH2 NH
110 I -H _C 1 C Single bond NHSO2CH3 \NH2 NH
111 CH2CH ~\\ -H C1 C,! Single bond NH
112 CHCH2CH(CH3)2 -H C 1 C Single bond NHSO2CH3 \NH2 NH
113 -CHCH(CH3)2 -H C 1 C Single bond NHSO2CH3 \NH2 -CHC(CH3)3 /NH
1 14 1 -H _C ~ 1 C Single bond NHSO2CH3 \NH2 -CHCH(CH3)CH2CH3 ~ NH
1 15 1 H -C ~ 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Comvpoound R1 D-(CH)R,-E-R4 -R2 -R3 n A Broken line ~ \ _ NH
116 -CHCH2 F -H C 1 C Single bond NHSO2CH3 \NH2 CH(CH2)4COOEt -H 117 I -H _C 1 C Single bond NHSO2Me NH2 -CH(CH2)2 NH
118 I COOCH2 -H -C~~ 1 C Single bond ~
NH
119 -CH(CH2)2 -H _C 1 C Single bond ~ -~ N H
120 -CH(CH2)2 COOH _H C1 C Single bond NHSO2CH3 ~NH2 NH
121 -CHCH2O T/\\ COOCH2 -H C1 C Single bond NHSO2CH3 ~NH2 NH
122 -CHCH2O 4~\ COOH -H C1 C Single bond NHSO2CH3 \NH2 -CHCH2O ?) NH
123 -H C// 1 C Single bond Table 1 (continued) Compound R1 (D(cH)mER4) -R2 -R3 n A Broken line 124 CHCH2O _H _C// NH 1 C Single bond NHSO2CH3 COOH \NH2 125 -CHCH2CH2 -H -C;~ 1 C Single bond NH
126 -CHCH2 /~1 -CI -H C1 C Single bond NHSO2CH3 \NH2 NH
127 -CHCH2CH2-C}COOCH3 -H C// 1 C Single bond NHSO2CH3 \NH2 COOH NH
128 -CHCH2 o -H _C 1 C Single bond NHS02CH i NH2 NH
129 CHCH2O /\ CH3 -H C//
1 C Single bond NHSO2CH3 \NH2 COOH NH
130 -CHCH2O -H _C// 1 C Single bond I \Ny2 COOCH2 \ NH
131 -CHCH2O /_~ -H _C// 1 C Single bond I \NH2 Table 1 (continued) Compound D-(CH)m-E-R4 No. R1 1 5 -R2 -R3 n A Broken line R
NH
132 CHCH2S-C> -H C~~ 1 C Single bond NHSO2CH3 \NH2 NH
133 -CHCH2S 4\_ OCH3 -H C1 C Single bond NHSO2CH3 \NH2 134 -CHCH2S-H -C\ 1 C Single bond NH
135 ~H H -H -C// 1 C Single bond NHSO2- C~ I NH2 -CHCH2-{ H ) NH
136 1 ~ -H -C 1 C Single bond NHSO2 \NH
i -"
~-\ NH
137 CH -H ,i -C 1 C Single bond NHS02 ~\> NH2 -CHCH2 ~_\ NH
138 -H C 1 C Single bond NHSO2--C~ \NH2 Table 1 (continued) Compound 1D-(CH)m-E-R4 R2--[ -R3 n A Broken line No. R R5 /\ NH
C 1 C Single bond NHSO \NH2 -CHCH2/\ OH NH
140 -H C// 1 C Single bond /-\
141 -CHCH2 COOH -H NH C1 C Single bond NHS02-~D
\NH2 -CHCH2C(CH3)3 NH
142 1 / -H _C// 1 C Single bond \NH2 143 I ~v\ -H C// 1 C Single bond NHS02 , \NH2 / \
1 C Single bond NHSOz --~~ \NH
COOH
NH
145 -CHCH2O -H C 1 C Single bond NHSO2-~_ \NH
Table 1 (continued) Compoound R-~ (-D-(CH)m-E-R4 -R2 v -R3 n A Broken line 146 I ~~ -H _C 1 C Single bond \NH2 -CHCH S NH
147 i 2~ -H _C1 C Single bond NHSO2 ---~~ \NH2 NH
148 CHCH2 I -H C 1 C Single bond NHSO2CH2COOH \NH2 NH
149 -CHCH2 -H _C 1 C Single bond NHSO2CH2COOH \NH2 NH
150 -CHCH2 4_\ -OH -H C1 C Single bond NHSO2CH2COOH \NH2 -- I -NH
151 -CHCH2C(CH3)3 -H C1 C Single bond NHSO2CH2COOH \NH2 152 CH(CH2)4CH3 --T // NH
i -H -C 1 C Single bond NHSO2CH2COOH \NH2 NH
153 -CHCH2O-//-\\' -H _C 1 C Single bond NHSO2CH2COOH \NH2 --- ---~ ; ~NH
154 -CHCH2O--C~ -H C/ 1 C Single bond NHSO2CH2COOH \NH2 Table 1 (continued) Compound 1-D-(CH)m-E-R4 R2 -R3 n A Broken line No. -R R5 ~ -~
1 C Single bond NHSO2CH2COOH \NH2 1 -('HCH2S H NH
56 -H _C 1 C Single bond NHSO2CH2COOH ~NH2 NH
157 -CHCH2{> -H C1 C Single bond NHSO2CF3 \NH2 -CHCH2 --\\ N H
158 -H C~~ 1 C Single bond NHSO2CF3 \NH2 159 -CHCH2-{~ ) -H _C 1 C Single bond NHSO2CF~3-- NH2 160 -CHCH2 C5 -H _C 1 C Single bond I
~~ NH
161 -H C1 C Single bond NHSO2CF3 \NH2 COOH NH
162 -CHCH2- -H -C// 1 C Single bond I
NHSO2CF3 \NH2 Table 1 (continued) Compound -R1 (D(CH)mER4 -R2 -R3 n A Broken line OH NH
163 -CHCH2 4/~\ -H -C// 1 C Single bond i \NH2 NH
164 -CH2CH(CH2)3CHq -H -C// 1 C Single bond NHSO2CF3 \NH2 165 CHCH2C(CH3)3 -H -C// NH 1 C Single bond NHS02CFg \NH2 NH
166 -CHCH2O-C\ -H -C// 1 C Single bond NHSO2CF3 \NH2 NH
167 CHCH2S{~ -H -C// 1 C Single bond I
NHSO2CF3 \NH2 NH
1 C Single bond 169 i -H -C 1 C Single bond NHSO2CH2 //_~\ NH2 CHCH2C(CH3)3 ~NH
170 i -H -C / 1 C Single bond \NH2 z140598 Table 1 (continued) Compound -D-(CH)m-E-R
No. R~ ~ 5 R2 -R3 n A Broken line R
171 -CHCH2O- (D NH
1 , -H -C 1 C Single bond i H f-C1 C Single bond NHSO2CH2 /\ I NH2 N H
173 -CHCH2 H -H C// 1 C Single bond NH2 ~NH2 NH
174 -CHCH2 -H C1 C Single bond NH2 \NH2 175 -CHCH2 -H -C1 C Single bond NH2 ~NH2 NH
176 -CHCH2 ~_~ CH;?COOH -H C1 C Single bond 177 -CHCH2 -H C 1 C Single bond I
NH2 ~NH2 ~
178 -CHCH24 COOH _H N H C 1 C Single bond Table 1 (continued) Compound (D(CH)mER4) No. R1 I -R2 -R3 n A Broken line CH(CH2)4CH3 NH
179 I -H -C~~ 1 C Single bond \NH2 -CHCH2C(CH3)3 ~ NH
180 1 -H -C ~ 1 C Single bond NH2 \NH2 NH
181 -CHCH2O 4~
~ -H -C 1 C Single bond NH2 \NH2 ~-~
1 C Single bond NH2 \NH2 ~
X:~ -H _C 1 C Single bond NH2 \NH2 184 CHCH2S -H C// NH 1 C Single bond NH2 ~NH2 CI ~T NH
185 -CHCH2S O -H _C// 1 C Single bond I
NH
-C 1 C Single bond NH2 \NH2 NH
187 -CH H -H I _C 1 C Single bond NHCH3 \NH2 Table 1 (continued) Compound D-(CH)m-E-R4 No. -R1 I R2 R3 n A Broken line R' NH
188 -CHCH2 H -H C1 C Single bond NHC2H5 \
- - -~.~ NH2 189 -H C1 C Single bond NHCH3 \NH2 190 -CHCH2 (~ -H C 1 C Single bond NH
191 -CHCH2 ( ~COOH -H C// 1 C Single bond NHCH3 \NH
-CHCH2C(CH3)3 NH
192 1 -H -C// 1 C Single bond NHCH3 \
2 ~~ /N H
193 CHCH O -H C/ 1 C Single bond NHCH3 \NH2 ~ NH
1 g4 -CHCH2SH -H C1 C Single bond NHCH3 \NH2 -CHCH2-{ H ) NH
195 I ~-/ -H _C1 C Single bond NHCH2-- C~\ NH2 Table 1 (continued) Compound (-D-(CH)m-E-R4) Broken line No. -R~ I 5 "R2 -R3 n A
R
-CHCH2 /_~ // NH
196 I ~-~ -H -C 1 C Single bond NHCH2--(~ \NH2 -CH2CH(CH2)3CH3 NH
197 1 /~ -H -C 1 C Single bond \NH2 198 -CHCH2C(CH3)3 -H // NH
/ ~ "C 1 C Single bond \NH2 -CHCH2OC2H; NH
199 1 -H -C1 C Single bond \NH2 200 NHCH /\) -H -C 1 C Single bond 2 \NH2 NH
\NH2 NH
\NH2 NH
203 -CH2-~H -H -C// 1 C
\NH2 NH
204 -(CH2)2CH3 -H -C// 1 C
\NH2 Table 1 (continued) Compound 1-D-(CH)m-E-R4 _R2 -R3 n A Broken line No. -R R5 NH
205 -CH2O (\ -H _C// C
\NH2 206 ~-~ -H C 1 C
-CH20 \NH2 207 -CH O ~ ~ -H -C// C
2 \NH2 NH
208 -CH20 r_N Ci -H _C// 1 c \NH2 2 \NH2 OH NH
2 \NH2 NH
211 -CH2O J/_\\ CH2COOH -H -C// 1 C
\NH2 \NH2 COOH NH
\NH2 Table 1 (continued) Compound -D-(CH)m-E-R4 No. -R1 5 -R2 -R3 n A Broken line R
NH
214 -CH2O ( -~ COOCH3 -H _C// 1 C
\NH2 2 \NH2 NH
217 -CH2S -H _C// 1 C
\NH2 NH
218 -CH2S 1 ~ OH -H _C// 1 C
\NH2 NH
219 -CH2S r\ COOH -H _C// 1 C
\NH2 NH
220 -CH2S COCH3 -H _C// 1 C
\NH2 NH
221 -CH -~ -H C1 C
I
OH \NH2 222 -CHCH2--( H -H C~NH 1 C
OCOCH3 ~ \NH2 Table 1 (continued) Compound 1(-D-(CH)rn-E-R4) _R2 -R3 I A Broken line No. -R R5 OCOC2H5 \NH2 224 -CHCH2-{ H ) -H // NH 1 C
I ~ -C
OCOOCH3 \NH2 225 -CHCH2--C~ -H CNH 1 C
NHCHO \NH2 226 -CHCH2-~~) -H -C// NH 1 C
NHCOOCH3 \NH2 227 -CHCH2--Ho -H // NH 1 C
I C
NHCOOC2H5 ~NH2 - -~- ~
~ NH
228 -CH -( H ) -H -C 1 C
NHCOOCH(CH3)2 \NH2 -CHCH2 < H ) // NH
229 1 ~--i -H -C 1 C
NHCOOCH2-4/- \NH2 230 -CHCH2-{ ~{ > -H C// NH 1 C
NHSO2CH3v \NH2 Table 1 (continued) Compound D-(CH)m-E-R4 No. -R1 I -R2 -R3 n A Broken line 231 -CHCH2- -H C~NH 1 C
NHSO2C2`H5 \NH2 - i _ 232 -CHCH2-( H ) -H NH
NHSO2 vC\NH 1 C
NHSO2COOH \NH2 234 -CHCH2--Ho -H C// NH 1 C
NH2 \NH2 CH NH
OH \NH2 236 -CHCH2 /\ OH -H CNH 1 C
OH \NH2 NH
NHSO2CH3 \NH2 238 -CH / ~ // NH
NHCOOC2H5 \NH2 Table 1 (continued) Compound R1 -D-(CH)m-E-R4 _R2 _R3 n A Broken line No. R5 -CHCH2C(CH3)3 //NH
NHSO2CH3 \NH
240 -CHCH2OC(CH3)3 -H CNH 1 C
NHCOOC2H5 \NH2 NH
241 -CHCH(CH3)2 -H C 1 C
NHSO2CH3 \NH2 -CHCH(CH3)2 //NH
242 1 H _C 1 C
NHCOOC2H5 \NH 1 NH
243 -CHC(CH3)3 -H C 1 C
NHSO2CH3 \NH
244 -CHC(CH3)3 -H C//NH 1 C
NHCOOC2H5 \NH
-CH(CH2)3CH3 //NH
NHSO2CH3 \NH2 NHSO2CH3 \NH2 214059g Table 1 (continued) Compound D-(CH)m-E-R4 No. -R1 I 5 -R2 F -R3 n A Broken line R
247 -CHCH2--C) -H ~ 1 C
NH
-C
OCOCH3 \NH2 248 -CHCH2 4~ NH 1 C
-H -C
OCOOC2H5 \NH2 249 -CHCH2 C\ COOH -H C11NH 1 C
OCOOC2H5 \NH2 250 -CHCH2 ( NH 1 C
-H -C
NHSO2CH3 \NH2 251 -CHCH2CH2 -H -C\ 1 C
NHSO2 \NH2 NH
253 -CHCH2 4\ -H C11 1 C
NHSO2CH2COQH \NH2 ~
I
NHCHO \NH2 Table 1 (continued) Compound -R1 (D(GH)mER4) _R2 -R3 n A Broken line No. R5 255 - I _ CHCH2 / ~ -F -H -C NH 1 C
NHCOOC2H5 \NH2 I \NH2 NHCOOCH2 ~/~\
257 -CHCH2-C~~ -H -C// 1 C
NH
NH2 \NH2 -CHCH2C(CH3)3 NH
258 ~H -H -C 1 C
\NH2 -CH(CH2)4CH3 NH
\NH2 -CHC(SCH3)(CH3)2 NH
260 1 -H -C// 1 c OCOOC2H5 \NH2 -CHCH2C(CH3)3 // NH
261 I OCONHCH2CH=CH2 H -C 1 C
\NH2 -CH(CH2)3CH3 NH
\NH2 -CHCH2C(CH3)3 NH
\NH2 __ Table 1 (continued) Compound -R1 (D(GH)mER4) -R2 -R3 n A Broken line No.
264 -CHCH2CH(C2H5)2 -H //NH -C 1 C
NHCOOC2H5 ~NH2 265 -CHCH2C(CH3)3 -H C//NH C
NHCOOCH(CH3)2 ~NH2 266 -CHCH2C(CH3)3 -H C// NH 1 C
NHCOOC(CH3)3 ~NH2 -CH(CH2)4CH3 NH
267 NHCOOCH2~~ -H -C\ C
268 -CH2CH(CH2)2CH3 -H //NH 1 C
C
NHSO2CH3 ~NH2 -CHCH2CH(CH3)2 -H CNH
NHSO2CH3 ~NH2 -CHCH2C(CH3)3 NH
NHSO2~' \ NH2 271 -CH2CH(CH2)2CH3 -H // NH 1 C
C
NH2 ~NH2 NH
272 -(CH2)2 /\ -H -C// 1 N
NH
47 -(CH2)4CH3 -H C 1 C Single bond \NH2 NH
48 -CH2CH2C (CH3)3 -H -C// 1 C Single bond \NH2 NH
49 -(CH2)9CH3 -H -C/~ 1 C Single bond \NH2 NH
50 -CH2Si(CH3)3 -H _C 1 C Single bond \NH2 NH
51 -CH2CH2Si(CH3)3 -H -C// 1 C Single bond \NH2 NH 52 -CH2OCH3 -H -C// 1 C Single bond \NH2 NH
53 CH2O ~-H _C// 1 C Single bond \NH2 NH
54 -CH2O--~ -H _C// 1 C Single bond `-/ \NH2 NH
55 -CH2OCH2 - -H -C// 1 C Single bond \NH2 NH
56 -CH2OH -H _C// 1 C Single bond \NH2 NH
57 -CH2SCH3 -H -C// 1 C Single bond \NH2 _.
21.40598 Table 1 (continued) Compound -R1 D-(CH)m-E=R4 -R2 -R3 n A Broken line NH
58 -CH2S r\ -H -C 1 C Single bond \NH2 NH
59 -CH2S -H -C// 1 C Single bond \NH2 NH
60 -CH2SCH2 - C~ -H -C// 1 C Single bond \NH2 NH
61 -CH2SO-r) -H -C// 1 C Single bond \NH2 NH
62 -CH2SO--O -H -C 1 C Single bond \NH2 NH
63 -CH2SO2-H -C// 1 C Single bond \NH2 NH
64 -CH2SO2H> -H -C 1 C Single bond \NH2 NH
65 -CH2CO {~ `> -H -C 1 C Single bond ~--~ \NH2 NH
66 -CH2CO-O -H -C// 1 C Single bond \NH2 NH
67 -CH2COOH -H -C// 1 C Single bond \NH2 NH
68 -CH2COOCH3 -H -C// 1 C Single bond \NH2 Table 1 (continued) Comvpoound R-1 (-D-(cH)m-E-R4) _R2 -R3 n A Broken line NH
69 -CH2NHCH3 -H _C// 1 C Single bond \NH2 NH
70 -CH2NH ~~\ -H C 1 C Single bond \NH2 NH
71 -CH2NH-H) -H _C// 1 C Single bond ~ \NH2 NH
72 -CH2NHCH2 -C~ -H _C// 1 C Single bond \NH2 NH
73 -CH2NHCOOCH3 -H _C// 1 C Single bond \NH2 NH
74 CH2NHCO /-H C// 1 C Single bond \NH2 NH
75 -CH2NHCO-<~H) -H C// 1 C Single bond \NH2 NH
76 -CH2NHCOOCH2 -H _C 1 C Single bond -~
NH
77 -CH2NHSO2 - L~ -H -C 1 C Single bond S
- NH
78 -CH2NHSO2CH3 -H C 1 C Single bond -'-- -- - - -NH
79 -CH2NHSO2 -{~ -H _C 1 C Single bond Table 1 (continued) Compound (-D-(cH)m-E-R4) -R2 -R3 o -R1 n A Broken line NH
80 -CH2NHSO2CH2 -H _C// 1 C Single bond \NH2 NH
81 -CH2NHSO2 {H~ -H -C// 1 C Single bond \NH2 -(- NH
82 -CH-O -H -C// 1 C Single bond OH \NH2 -CHCH2C(CH3)g // NH
83 I -H _C 1 C Single bond OH \NH2 NH
84 -CH -H G// 1 C Single bond OSi(CH3)3 \NH2 ---- ----- -~--CHCH2C(CH3)3 NH
85 I -H _G 1 C Single bond O-CH3 \NH2 - -~-- --CHCH2C(CH3)3 NH
86 O/-~ -H 1 C Single bond O \NH2 _T -NH
87 -CH ~~ -H -C//
1 C Single bond NH
88 -H C// 1 C Single bond OCOCH3 \NH2 21~0598 Table 1 (continued) Compound R-1 (D(CH)mER4) -R2 -R3 I A Broken line -CHCH2C(CH3)3 /NH
89 I -H -C ~ 1 C Single bond OCOOCH3 \NH2 NH
90 -~H~ -H C// 1 C Single bond OCONH2 \NH2 NH
91 -CH /_ -H C// 1 C Single bond -CHCH2C(CH3)3 /NH
92 I -H -C ~ 1 C Single bond OCON(CH3)2 \NH2 93 -CH2CH-CH~ / NH
-H C 1 C Single bond OCONHCH2CH=CH2 NH2 NH
94 -CHCH2~ ~ ~ TH _C 1 C Single bond NHCHO \NH2 - ---~---I- - NH -CHCH2C(CH3)3 95 I -H C 1 C Single bond NHCOCH3 \NH
~ NH
96 CHCH2-< H;> -H C 1 C Single bond NHCOCF3~--~ \NH2 -- ---,--.--- -97 CHCH2 H _C// NH
1 C Single bond NHCOOCH3 \NH2 _ ,._ Table 1 (continued) Compound Ri (-D-(CH)m-E-R4'\ _R2 -R3 n A Broken line No. R5 CHC(SCH3)(CH3)2 // NH
98 -H C 1 C Single bond NHCOOC2H5 \NH2 NH
99 -CH H -H C1 C Single bond NHCO-C~ NH2 2 ~ ~ NH
100 -CH CH -H C1 C Single bond NHCO-<~ NH2 -CHCH2C(CH3)3 NH
101 I ~~ -H -C~~ 1 C Single bond \NH2 NH
102 -CHCH2 -H C 1 C Single bond NHCOOCH2CH=CH2 ~NH2 NH
103 -CHCH2 (\ COOH -H C// 1 C Single bond -CHCH2C(CH3)3 /NH
104 ~ -H -C ~ 1 C Single bond NH
105 ~H -H 1 C Single bond C
NHSO2CH3 \NHz __ Table 1 (continued) Compoound R' (DH)m.ER4) -R2 -R3 n A Broken line NH
106 -CHCH2- C -H C1 C Single bond NH
107 -CH /~\ -H _C1 C Single bond NHSO2CH3 ~NH2 NH
108 -CHCH2 () -H C 1 C Single bond NHSO2CH3 ~NH2 NH
-CH(CH2)3CH3 109 1 -H _C 1 C Single bond NHSO2CH3 \NH2 NH
110 I -H _C 1 C Single bond NHSO2CH3 \NH2 NH
111 CH2CH ~\\ -H C1 C,! Single bond NH
112 CHCH2CH(CH3)2 -H C 1 C Single bond NHSO2CH3 \NH2 NH
113 -CHCH(CH3)2 -H C 1 C Single bond NHSO2CH3 \NH2 -CHC(CH3)3 /NH
1 14 1 -H _C ~ 1 C Single bond NHSO2CH3 \NH2 -CHCH(CH3)CH2CH3 ~ NH
1 15 1 H -C ~ 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Comvpoound R1 D-(CH)R,-E-R4 -R2 -R3 n A Broken line ~ \ _ NH
116 -CHCH2 F -H C 1 C Single bond NHSO2CH3 \NH2 CH(CH2)4COOEt -H 117 I -H _C 1 C Single bond NHSO2Me NH2 -CH(CH2)2 NH
118 I COOCH2 -H -C~~ 1 C Single bond ~
NH
119 -CH(CH2)2 -H _C 1 C Single bond ~ -~ N H
120 -CH(CH2)2 COOH _H C1 C Single bond NHSO2CH3 ~NH2 NH
121 -CHCH2O T/\\ COOCH2 -H C1 C Single bond NHSO2CH3 ~NH2 NH
122 -CHCH2O 4~\ COOH -H C1 C Single bond NHSO2CH3 \NH2 -CHCH2O ?) NH
123 -H C// 1 C Single bond Table 1 (continued) Compound R1 (D(cH)mER4) -R2 -R3 n A Broken line 124 CHCH2O _H _C// NH 1 C Single bond NHSO2CH3 COOH \NH2 125 -CHCH2CH2 -H -C;~ 1 C Single bond NH
126 -CHCH2 /~1 -CI -H C1 C Single bond NHSO2CH3 \NH2 NH
127 -CHCH2CH2-C}COOCH3 -H C// 1 C Single bond NHSO2CH3 \NH2 COOH NH
128 -CHCH2 o -H _C 1 C Single bond NHS02CH i NH2 NH
129 CHCH2O /\ CH3 -H C//
1 C Single bond NHSO2CH3 \NH2 COOH NH
130 -CHCH2O -H _C// 1 C Single bond I \Ny2 COOCH2 \ NH
131 -CHCH2O /_~ -H _C// 1 C Single bond I \NH2 Table 1 (continued) Compound D-(CH)m-E-R4 No. R1 1 5 -R2 -R3 n A Broken line R
NH
132 CHCH2S-C> -H C~~ 1 C Single bond NHSO2CH3 \NH2 NH
133 -CHCH2S 4\_ OCH3 -H C1 C Single bond NHSO2CH3 \NH2 134 -CHCH2S-H -C\ 1 C Single bond NH
135 ~H H -H -C// 1 C Single bond NHSO2- C~ I NH2 -CHCH2-{ H ) NH
136 1 ~ -H -C 1 C Single bond NHSO2 \NH
i -"
~-\ NH
137 CH -H ,i -C 1 C Single bond NHS02 ~\> NH2 -CHCH2 ~_\ NH
138 -H C 1 C Single bond NHSO2--C~ \NH2 Table 1 (continued) Compound 1D-(CH)m-E-R4 R2--[ -R3 n A Broken line No. R R5 /\ NH
C 1 C Single bond NHSO \NH2 -CHCH2/\ OH NH
140 -H C// 1 C Single bond /-\
141 -CHCH2 COOH -H NH C1 C Single bond NHS02-~D
\NH2 -CHCH2C(CH3)3 NH
142 1 / -H _C// 1 C Single bond \NH2 143 I ~v\ -H C// 1 C Single bond NHS02 , \NH2 / \
1 C Single bond NHSOz --~~ \NH
COOH
NH
145 -CHCH2O -H C 1 C Single bond NHSO2-~_ \NH
Table 1 (continued) Compoound R-~ (-D-(CH)m-E-R4 -R2 v -R3 n A Broken line 146 I ~~ -H _C 1 C Single bond \NH2 -CHCH S NH
147 i 2~ -H _C1 C Single bond NHSO2 ---~~ \NH2 NH
148 CHCH2 I -H C 1 C Single bond NHSO2CH2COOH \NH2 NH
149 -CHCH2 -H _C 1 C Single bond NHSO2CH2COOH \NH2 NH
150 -CHCH2 4_\ -OH -H C1 C Single bond NHSO2CH2COOH \NH2 -- I -NH
151 -CHCH2C(CH3)3 -H C1 C Single bond NHSO2CH2COOH \NH2 152 CH(CH2)4CH3 --T // NH
i -H -C 1 C Single bond NHSO2CH2COOH \NH2 NH
153 -CHCH2O-//-\\' -H _C 1 C Single bond NHSO2CH2COOH \NH2 --- ---~ ; ~NH
154 -CHCH2O--C~ -H C/ 1 C Single bond NHSO2CH2COOH \NH2 Table 1 (continued) Compound 1-D-(CH)m-E-R4 R2 -R3 n A Broken line No. -R R5 ~ -~
1 C Single bond NHSO2CH2COOH \NH2 1 -('HCH2S H NH
56 -H _C 1 C Single bond NHSO2CH2COOH ~NH2 NH
157 -CHCH2{> -H C1 C Single bond NHSO2CF3 \NH2 -CHCH2 --\\ N H
158 -H C~~ 1 C Single bond NHSO2CF3 \NH2 159 -CHCH2-{~ ) -H _C 1 C Single bond NHSO2CF~3-- NH2 160 -CHCH2 C5 -H _C 1 C Single bond I
~~ NH
161 -H C1 C Single bond NHSO2CF3 \NH2 COOH NH
162 -CHCH2- -H -C// 1 C Single bond I
NHSO2CF3 \NH2 Table 1 (continued) Compound -R1 (D(CH)mER4 -R2 -R3 n A Broken line OH NH
163 -CHCH2 4/~\ -H -C// 1 C Single bond i \NH2 NH
164 -CH2CH(CH2)3CHq -H -C// 1 C Single bond NHSO2CF3 \NH2 165 CHCH2C(CH3)3 -H -C// NH 1 C Single bond NHS02CFg \NH2 NH
166 -CHCH2O-C\ -H -C// 1 C Single bond NHSO2CF3 \NH2 NH
167 CHCH2S{~ -H -C// 1 C Single bond I
NHSO2CF3 \NH2 NH
1 C Single bond 169 i -H -C 1 C Single bond NHSO2CH2 //_~\ NH2 CHCH2C(CH3)3 ~NH
170 i -H -C / 1 C Single bond \NH2 z140598 Table 1 (continued) Compound -D-(CH)m-E-R
No. R~ ~ 5 R2 -R3 n A Broken line R
171 -CHCH2O- (D NH
1 , -H -C 1 C Single bond i H f-C1 C Single bond NHSO2CH2 /\ I NH2 N H
173 -CHCH2 H -H C// 1 C Single bond NH2 ~NH2 NH
174 -CHCH2 -H C1 C Single bond NH2 \NH2 175 -CHCH2 -H -C1 C Single bond NH2 ~NH2 NH
176 -CHCH2 ~_~ CH;?COOH -H C1 C Single bond 177 -CHCH2 -H C 1 C Single bond I
NH2 ~NH2 ~
178 -CHCH24 COOH _H N H C 1 C Single bond Table 1 (continued) Compound (D(CH)mER4) No. R1 I -R2 -R3 n A Broken line CH(CH2)4CH3 NH
179 I -H -C~~ 1 C Single bond \NH2 -CHCH2C(CH3)3 ~ NH
180 1 -H -C ~ 1 C Single bond NH2 \NH2 NH
181 -CHCH2O 4~
~ -H -C 1 C Single bond NH2 \NH2 ~-~
1 C Single bond NH2 \NH2 ~
X:~ -H _C 1 C Single bond NH2 \NH2 184 CHCH2S -H C// NH 1 C Single bond NH2 ~NH2 CI ~T NH
185 -CHCH2S O -H _C// 1 C Single bond I
NH
-C 1 C Single bond NH2 \NH2 NH
187 -CH H -H I _C 1 C Single bond NHCH3 \NH2 Table 1 (continued) Compound D-(CH)m-E-R4 No. -R1 I R2 R3 n A Broken line R' NH
188 -CHCH2 H -H C1 C Single bond NHC2H5 \
- - -~.~ NH2 189 -H C1 C Single bond NHCH3 \NH2 190 -CHCH2 (~ -H C 1 C Single bond NH
191 -CHCH2 ( ~COOH -H C// 1 C Single bond NHCH3 \NH
-CHCH2C(CH3)3 NH
192 1 -H -C// 1 C Single bond NHCH3 \
2 ~~ /N H
193 CHCH O -H C/ 1 C Single bond NHCH3 \NH2 ~ NH
1 g4 -CHCH2SH -H C1 C Single bond NHCH3 \NH2 -CHCH2-{ H ) NH
195 I ~-/ -H _C1 C Single bond NHCH2-- C~\ NH2 Table 1 (continued) Compound (-D-(CH)m-E-R4) Broken line No. -R~ I 5 "R2 -R3 n A
R
-CHCH2 /_~ // NH
196 I ~-~ -H -C 1 C Single bond NHCH2--(~ \NH2 -CH2CH(CH2)3CH3 NH
197 1 /~ -H -C 1 C Single bond \NH2 198 -CHCH2C(CH3)3 -H // NH
/ ~ "C 1 C Single bond \NH2 -CHCH2OC2H; NH
199 1 -H -C1 C Single bond \NH2 200 NHCH /\) -H -C 1 C Single bond 2 \NH2 NH
\NH2 NH
\NH2 NH
203 -CH2-~H -H -C// 1 C
\NH2 NH
204 -(CH2)2CH3 -H -C// 1 C
\NH2 Table 1 (continued) Compound 1-D-(CH)m-E-R4 _R2 -R3 n A Broken line No. -R R5 NH
205 -CH2O (\ -H _C// C
\NH2 206 ~-~ -H C 1 C
-CH20 \NH2 207 -CH O ~ ~ -H -C// C
2 \NH2 NH
208 -CH20 r_N Ci -H _C// 1 c \NH2 2 \NH2 OH NH
2 \NH2 NH
211 -CH2O J/_\\ CH2COOH -H -C// 1 C
\NH2 \NH2 COOH NH
\NH2 Table 1 (continued) Compound -D-(CH)m-E-R4 No. -R1 5 -R2 -R3 n A Broken line R
NH
214 -CH2O ( -~ COOCH3 -H _C// 1 C
\NH2 2 \NH2 NH
217 -CH2S -H _C// 1 C
\NH2 NH
218 -CH2S 1 ~ OH -H _C// 1 C
\NH2 NH
219 -CH2S r\ COOH -H _C// 1 C
\NH2 NH
220 -CH2S COCH3 -H _C// 1 C
\NH2 NH
221 -CH -~ -H C1 C
I
OH \NH2 222 -CHCH2--( H -H C~NH 1 C
OCOCH3 ~ \NH2 Table 1 (continued) Compound 1(-D-(CH)rn-E-R4) _R2 -R3 I A Broken line No. -R R5 OCOC2H5 \NH2 224 -CHCH2-{ H ) -H // NH 1 C
I ~ -C
OCOOCH3 \NH2 225 -CHCH2--C~ -H CNH 1 C
NHCHO \NH2 226 -CHCH2-~~) -H -C// NH 1 C
NHCOOCH3 \NH2 227 -CHCH2--Ho -H // NH 1 C
I C
NHCOOC2H5 ~NH2 - -~- ~
~ NH
228 -CH -( H ) -H -C 1 C
NHCOOCH(CH3)2 \NH2 -CHCH2 < H ) // NH
229 1 ~--i -H -C 1 C
NHCOOCH2-4/- \NH2 230 -CHCH2-{ ~{ > -H C// NH 1 C
NHSO2CH3v \NH2 Table 1 (continued) Compound D-(CH)m-E-R4 No. -R1 I -R2 -R3 n A Broken line 231 -CHCH2- -H C~NH 1 C
NHSO2C2`H5 \NH2 - i _ 232 -CHCH2-( H ) -H NH
NHSO2 vC\NH 1 C
NHSO2COOH \NH2 234 -CHCH2--Ho -H C// NH 1 C
NH2 \NH2 CH NH
OH \NH2 236 -CHCH2 /\ OH -H CNH 1 C
OH \NH2 NH
NHSO2CH3 \NH2 238 -CH / ~ // NH
NHCOOC2H5 \NH2 Table 1 (continued) Compound R1 -D-(CH)m-E-R4 _R2 _R3 n A Broken line No. R5 -CHCH2C(CH3)3 //NH
NHSO2CH3 \NH
240 -CHCH2OC(CH3)3 -H CNH 1 C
NHCOOC2H5 \NH2 NH
241 -CHCH(CH3)2 -H C 1 C
NHSO2CH3 \NH2 -CHCH(CH3)2 //NH
242 1 H _C 1 C
NHCOOC2H5 \NH 1 NH
243 -CHC(CH3)3 -H C 1 C
NHSO2CH3 \NH
244 -CHC(CH3)3 -H C//NH 1 C
NHCOOC2H5 \NH
-CH(CH2)3CH3 //NH
NHSO2CH3 \NH2 NHSO2CH3 \NH2 214059g Table 1 (continued) Compound D-(CH)m-E-R4 No. -R1 I 5 -R2 F -R3 n A Broken line R
247 -CHCH2--C) -H ~ 1 C
NH
-C
OCOCH3 \NH2 248 -CHCH2 4~ NH 1 C
-H -C
OCOOC2H5 \NH2 249 -CHCH2 C\ COOH -H C11NH 1 C
OCOOC2H5 \NH2 250 -CHCH2 ( NH 1 C
-H -C
NHSO2CH3 \NH2 251 -CHCH2CH2 -H -C\ 1 C
NHSO2 \NH2 NH
253 -CHCH2 4\ -H C11 1 C
NHSO2CH2COQH \NH2 ~
I
NHCHO \NH2 Table 1 (continued) Compound -R1 (D(GH)mER4) _R2 -R3 n A Broken line No. R5 255 - I _ CHCH2 / ~ -F -H -C NH 1 C
NHCOOC2H5 \NH2 I \NH2 NHCOOCH2 ~/~\
257 -CHCH2-C~~ -H -C// 1 C
NH
NH2 \NH2 -CHCH2C(CH3)3 NH
258 ~H -H -C 1 C
\NH2 -CH(CH2)4CH3 NH
\NH2 -CHC(SCH3)(CH3)2 NH
260 1 -H -C// 1 c OCOOC2H5 \NH2 -CHCH2C(CH3)3 // NH
261 I OCONHCH2CH=CH2 H -C 1 C
\NH2 -CH(CH2)3CH3 NH
\NH2 -CHCH2C(CH3)3 NH
\NH2 __ Table 1 (continued) Compound -R1 (D(GH)mER4) -R2 -R3 n A Broken line No.
264 -CHCH2CH(C2H5)2 -H //NH -C 1 C
NHCOOC2H5 ~NH2 265 -CHCH2C(CH3)3 -H C//NH C
NHCOOCH(CH3)2 ~NH2 266 -CHCH2C(CH3)3 -H C// NH 1 C
NHCOOC(CH3)3 ~NH2 -CH(CH2)4CH3 NH
267 NHCOOCH2~~ -H -C\ C
268 -CH2CH(CH2)2CH3 -H //NH 1 C
C
NHSO2CH3 ~NH2 -CHCH2CH(CH3)2 -H CNH
NHSO2CH3 ~NH2 -CHCH2C(CH3)3 NH
NHSO2~' \ NH2 271 -CH2CH(CH2)2CH3 -H // NH 1 C
C
NH2 ~NH2 NH
272 -(CH2)2 /\ -H -C// 1 N
NH
Table 1 (continued) Compound 1D-(CH)m-E-R4 -R2 -R3 n A Broken line No. -R R5 NH
274 CH ~-\ -H -C// 1 N
NHSO2CH3 \NH2 NH
275 -CHCH2-~) -H -C// 1 N
NHCHO \NH2 NH
NHSO2CH3 \NH2 277 -CHCH2 T\ ~NH
NHCOOC2H5 \NH2 278 -CHCH2 -H ~NH 1 N
-C
NH2 \NH2 NH
279 -CH2CH ~_\ -H C1 N II', NHSO2CH3 \NH2 280 -CHCH2 / \ -H // NH 1 N
-C
OCOOC2H5 \NH2 NH
OCONHCH2CH=CH2 \NH2 Table 1 (continued) Comvpoound R1 (D(GH)mBR4) -R2 -R3 n A Broken line NH
OH ~NH2 NH
NHSO2CH3 ~NH2 NH
284 -CHCH2-C~ -H -C// 1 N
- ---i NH
285 -CHCH2--C~ -H C 1 N
NH
C
NHCOOCH(CH3)2 NH2 NH
NHCOOC(CH3)3 \NH2 NH
288 -CHCH2-o -H -C// 1 N
NHCOOC(CH3)3 ~NH2 ~ NH
NHCO~OCH(CH3)2 \NHZ
274 CH ~-\ -H -C// 1 N
NHSO2CH3 \NH2 NH
275 -CHCH2-~) -H -C// 1 N
NHCHO \NH2 NH
NHSO2CH3 \NH2 277 -CHCH2 T\ ~NH
NHCOOC2H5 \NH2 278 -CHCH2 -H ~NH 1 N
-C
NH2 \NH2 NH
279 -CH2CH ~_\ -H C1 N II', NHSO2CH3 \NH2 280 -CHCH2 / \ -H // NH 1 N
-C
OCOOC2H5 \NH2 NH
OCONHCH2CH=CH2 \NH2 Table 1 (continued) Comvpoound R1 (D(GH)mBR4) -R2 -R3 n A Broken line NH
OH ~NH2 NH
NHSO2CH3 ~NH2 NH
284 -CHCH2-C~ -H -C// 1 N
- ---i NH
285 -CHCH2--C~ -H C 1 N
NH
C
NHCOOCH(CH3)2 NH2 NH
NHCOOC(CH3)3 \NH2 NH
288 -CHCH2-o -H -C// 1 N
NHCOOC(CH3)3 ~NH2 ~ NH
NHCO~OCH(CH3)2 \NHZ
Table 1 (continued) C Npound R-~ -D-(CH)R,-E-R4 -R2 -R3 n A Broken line NH
OH \NH2 I HCH2C(CH3)3 -H // NH 1 N
NHSO2CH3 \NH2 C
-CH(CH2)2SCH3 // NH
292 I -H _C 1 N
NHSO2CH3 \NH2 293 -CH(CH2)3CH3 -H //NH 1 N
NHSO2CH3 C\NH2 -CHC(SCH3)(CH3)2 //NH
NHCOOC2H5 \NH2 -CH(CH2)4CH3 NH
295 I -H _C// 1 N
NHSO2CH2COOH \NH2 296 -CHCH2C(CH3)3 -H //NH 1 N
NHCOOC2H5 C\NH2 297 -CHCH2C(CH3)3 H /NH 1 N
NHCOOCH(CH3)2 \NH2 C
-CHCH2CH(C2H5)2 //NH N
NHCOOC2H5 \NH2 299 -CHCH2C(CH3)3 -H // NH I N
NHCOOC(CH3)3 C\NH2 Table 1 (continued) Compound -R1 (D(CH)mER4' -R2 -R3 n A Broken line -CHCH2C(CH3)3 NH
300 NHCOOCH2 r\ -H -C/~ 1 N
\NH2 301 -CHCH2C(CH3)3 -H
OH \NH2 -CH(CH2)2COOH /NH
302 NHSO2 / ~ -H -C ~ 1 N
\NH2 NH
303 -CH ~ -H -C2 C Single bond NHSO2CH3 ~NH2 -CHCH2C(CH3)3 /NH
304 I -H -C 2 C Single bond NHSO2CH3 \NH2 NH
305 -CHCH2 -H C 2 C Single bond NHSO2CH3 ~NH2 NH
306 -CHCH2--C -H C// 2 C Single bond NHCOOC2H5 ~NH2 -CHCH2C(CH3)g // NH
307 ~ -H -C 2 C Single bond NHCOOC2H5 \NH
NH
308 -CHCH2-~) -H C2 C Single bond I
NHCOOC2H5 ~NH2 Table 1 (continued) Compound (-D-(CH)m-E-R4"
No. -R1 R5 R2 -R3 n A Broken line NH
309 -(CH2)3 -H -C// 2 C Single bond \NH2 ~ ~ NH
310 -CHCH2- -H C// 2 C Single bond NH2 \NH2 NH
311 -CH -H _C 2 C Single bond NHCOOCH(CH3)2 NH2 -CHCH2C(C2H5)2 NH
312 I -H _C~~ 2 C Single bond NHCOOC(CH3)3 \NH2 -CHCH2C(CH3)g // NH
313 I -H -C 2 C Single bond OH \NH2 -\ NH
314 - CH2CH4-H C// 2 C Single bond NHSO2CH3 \NH2 ~ NH
315 -CHCH2 > -H C 2 C Single bond OCOOC2H5 \NH2 NH
316 -CH-H -H _C// 2 C Single bond OH \NH2 317 -CHCH2--( -H CNH 2 C
NHSO2CH3 \NH2 Table 1 (continued) Comvpoound R1 D(CH)n,-E-R4 -R2 -R3 n A Broken line NH
318 -CH -H _C 2 C
NHCOOCH(CH3)2 \NH2 NH
NHSO2CH3 \NH2 NH
320 -CHCH2 -H _C 2 C
NHCOOC2H5 \NH2 321 -CHCH2C(CH3)3 -H _CNH 2 C
NHSO2CH3 \NH2 -CHCH2CH(C2H5)2 -H /NH 2 C
322 i _C
NHCOOC(CH3)3 \NH2 323 -CHCH2C(CH3)3 -H
C~NH 2 C
OH \NH2 NH
324 -CH -o -H _C 2 N
NHSO2CH3 \NH2 NH
325 -CHCH2--~ -H _C// 2 N
NHCOOC(CH3)3 \NH2 NH
326 -CHCH2-~ ~ -H -C 2 N
NHSO2CH3 \NH2 Table 1 (continued) Comvpoound -R1 (D*(CH)mER4 -R2 -R3 n A Broken line 327 -CHCH2 4\ //NH 2 N
i -H -C
OCOOC2H5 \NH2 328 -CHCH2C(CH3)3 -H C//NH 2 N
NHSO2CH3 \NH2 I H(CH2)2SCH3 3 -H C//NH 2 N
NHCOOCH(CH3)2 \NH2 330 -CHCH2C(CH3)3 -H _C// NH 2 N
OH \NH2 NH
331 -CHCH2---C> -CH3 -C// 1 C Single bond NHSO2CH3 ~NH2 NH
332 -CH-(D -CH3 _C 1 C Single bond NHCOOCH(CH3)2 \NH2 NH
333 -CHCH2 -CH3 C 1 C Single bond NHSO2CH3 ~NH2 ~ A C// NH
334 -CHCH2- _ -CH3 1 C Single bond OCOOC2H5 \NH2 NH
335 -CHCH2C(CH3) -CH3 C// 1 C Single bond OH \NH2 Table 1 (continued) Compound -R1 (-D-(cH)m-E-R4) _R2 -R3 I A Broken line -CHCH2CH(C2H5)2 /NH
336 1 -CH3 -C / 1 C Single bond NHCOOC(CH3)3 \NH2 -CHCH2C(CH 3)3 NH
337 ~ -CH3 _C 1 C Single bond NHSO2CH3 \NH2 NH
338 -CHCH2--C~ -CH3 -C// 1 C
NHSO2CH3 ~NH2 NH
339 -CH-~H -CH3 -C 1 C
NHCOOCH(CH3)2 \NH2 NH
340 -CHCH2 ~ A -CH3 _C 1 C
NHSO2CH3 ~NH2 NH
341 -CH2CH ~-~ -CH3 C 1 C
OCOOC2H5 \NH2 342 -CHCH2CH(C2H5)2 -CH3 C//NH 1 C
NHCOOC(CH3)3 \NH2 -C
I HCH2C(CH3)3 -CH3 CNH
NHSO2CH3 \NH2 344 -CHCH2C(CH3)3 -CH3 C//NH 1 C
OH \NH2 Table 1 (continued) Compound R1 (-D-(CH)m-E-R4' _R2 -R3 n A Broken line NH
345 -CI HCH2--C) -CH3 _C// 1 N
NHSO2CH3 \NH2 NH
346 -CH2CH ~~\ -CH3 C 1 N
NHCOOCH(CH3)2 NH2 NH
347 -CHCH2 ~ \ -CH3 C 1 N
NHSO2CH3 ~NH2 NH
348 -CH //\ -CH3 C 1 N
I _ OCOOC2H5 \NH2 349 -CHCH2C(CH3)3 -CH3 { CNH 1 N
NHSO2CH3 \NH2 350 -CHCH2CH(C2H5)2 -CH3 C~NH 1 N
NHCOOC(CH3)3 \NH ~
351 -CHCH2C(CH3)3 -CH3 C//NH 1 N
OH \NH2 NH
352 ~H -CH3 _C2 C Single bond NHSO2CH3 \NH2 NH
353 -CHCH2-(D -CH3 C 2 C Single bond NHCOOCH(CH3)2 \NH2 Table 1 (continued) Compound No. -R1 (D(CH)mER4) _R2 _R3 n A Brok en line CHCH2 r\ NH
354 -CH3 C~~ 2 C Single bond NHSO2CH3 \NH2 NH
355 C I _H2CH ~~ CH3 C//
2 C Single bond -CHCH2C(CH3)3 // NH
356 I -CH3 -C 2 C Single bond NHSO2CH3 \NH2 -CH(CH2)4CH3 /NH
357 ~ -CH3 _C ~ 2 C Single bond NHCOOC(CH3)3 \NH2 NH
358 -CHCH2CH(CH3)2 -CH3 C// 2 C Single bond OH \NH2 NH
NHSO2CH3 \NH2 ~--~ NH
360 -CHCH2-{ H -CH3 ? 2 C
~ ~ -C
NHCOOC2H5 \NH2 NH
361 -CHCH2-~) -CH3 -C2 C
I
NH
362 -CH2CH ~ ~ -CH3 C// 2 C
OCOOCH(CH3)2 \NH2 Table 1 (continued) Compound D-(CH)m-E-R4 2 3 No. -R1 R5 -R -R n A Broken line 363 -CHCH2C(CH3)3 -CH3 //NH
NHSO2CH3 \NH2 364 -CHC(SCH3)(CH3)2 -CH3 -C//NH 2 C
NHCOOC(CH3)3 ~NH2 365 -CHCH2CH(CH3)3 -CH3 C//NH 2 C
NH2 \NH2 NH
366 -CHCH2-CH~ -CH3 -C// 2 N
I
NHCOOC2H5 ~NH2 NH
367 -CHCH2--O -CH3 _C// 2 N
NHSO2CH3 ~NH2 NH
NHSO2CH3 ~NH2 - ~, NH
369 -CHCH2 r\~ COOH -CH3 C// 2 N
OCOOCH(CH3)2 ~NH2 -CHCH2C(CH3)i /NH/
370 CH3 , -C
\NH2 -CH(CH2)2SCH3 //NH
NHCOOC(CH3)3 \NH2 372 -CH2CH(CH2)3CH3 -CH3 ~NH 2 N
I -C
OH \NH2 I HCH2C(CH3)3 -H // NH 1 N
NHSO2CH3 \NH2 C
-CH(CH2)2SCH3 // NH
292 I -H _C 1 N
NHSO2CH3 \NH2 293 -CH(CH2)3CH3 -H //NH 1 N
NHSO2CH3 C\NH2 -CHC(SCH3)(CH3)2 //NH
NHCOOC2H5 \NH2 -CH(CH2)4CH3 NH
295 I -H _C// 1 N
NHSO2CH2COOH \NH2 296 -CHCH2C(CH3)3 -H //NH 1 N
NHCOOC2H5 C\NH2 297 -CHCH2C(CH3)3 H /NH 1 N
NHCOOCH(CH3)2 \NH2 C
-CHCH2CH(C2H5)2 //NH N
NHCOOC2H5 \NH2 299 -CHCH2C(CH3)3 -H // NH I N
NHCOOC(CH3)3 C\NH2 Table 1 (continued) Compound -R1 (D(CH)mER4' -R2 -R3 n A Broken line -CHCH2C(CH3)3 NH
300 NHCOOCH2 r\ -H -C/~ 1 N
\NH2 301 -CHCH2C(CH3)3 -H
OH \NH2 -CH(CH2)2COOH /NH
302 NHSO2 / ~ -H -C ~ 1 N
\NH2 NH
303 -CH ~ -H -C2 C Single bond NHSO2CH3 ~NH2 -CHCH2C(CH3)3 /NH
304 I -H -C 2 C Single bond NHSO2CH3 \NH2 NH
305 -CHCH2 -H C 2 C Single bond NHSO2CH3 ~NH2 NH
306 -CHCH2--C -H C// 2 C Single bond NHCOOC2H5 ~NH2 -CHCH2C(CH3)g // NH
307 ~ -H -C 2 C Single bond NHCOOC2H5 \NH
NH
308 -CHCH2-~) -H C2 C Single bond I
NHCOOC2H5 ~NH2 Table 1 (continued) Compound (-D-(CH)m-E-R4"
No. -R1 R5 R2 -R3 n A Broken line NH
309 -(CH2)3 -H -C// 2 C Single bond \NH2 ~ ~ NH
310 -CHCH2- -H C// 2 C Single bond NH2 \NH2 NH
311 -CH -H _C 2 C Single bond NHCOOCH(CH3)2 NH2 -CHCH2C(C2H5)2 NH
312 I -H _C~~ 2 C Single bond NHCOOC(CH3)3 \NH2 -CHCH2C(CH3)g // NH
313 I -H -C 2 C Single bond OH \NH2 -\ NH
314 - CH2CH4-H C// 2 C Single bond NHSO2CH3 \NH2 ~ NH
315 -CHCH2 > -H C 2 C Single bond OCOOC2H5 \NH2 NH
316 -CH-H -H _C// 2 C Single bond OH \NH2 317 -CHCH2--( -H CNH 2 C
NHSO2CH3 \NH2 Table 1 (continued) Comvpoound R1 D(CH)n,-E-R4 -R2 -R3 n A Broken line NH
318 -CH -H _C 2 C
NHCOOCH(CH3)2 \NH2 NH
NHSO2CH3 \NH2 NH
320 -CHCH2 -H _C 2 C
NHCOOC2H5 \NH2 321 -CHCH2C(CH3)3 -H _CNH 2 C
NHSO2CH3 \NH2 -CHCH2CH(C2H5)2 -H /NH 2 C
322 i _C
NHCOOC(CH3)3 \NH2 323 -CHCH2C(CH3)3 -H
C~NH 2 C
OH \NH2 NH
324 -CH -o -H _C 2 N
NHSO2CH3 \NH2 NH
325 -CHCH2--~ -H _C// 2 N
NHCOOC(CH3)3 \NH2 NH
326 -CHCH2-~ ~ -H -C 2 N
NHSO2CH3 \NH2 Table 1 (continued) Comvpoound -R1 (D*(CH)mER4 -R2 -R3 n A Broken line 327 -CHCH2 4\ //NH 2 N
i -H -C
OCOOC2H5 \NH2 328 -CHCH2C(CH3)3 -H C//NH 2 N
NHSO2CH3 \NH2 I H(CH2)2SCH3 3 -H C//NH 2 N
NHCOOCH(CH3)2 \NH2 330 -CHCH2C(CH3)3 -H _C// NH 2 N
OH \NH2 NH
331 -CHCH2---C> -CH3 -C// 1 C Single bond NHSO2CH3 ~NH2 NH
332 -CH-(D -CH3 _C 1 C Single bond NHCOOCH(CH3)2 \NH2 NH
333 -CHCH2 -CH3 C 1 C Single bond NHSO2CH3 ~NH2 ~ A C// NH
334 -CHCH2- _ -CH3 1 C Single bond OCOOC2H5 \NH2 NH
335 -CHCH2C(CH3) -CH3 C// 1 C Single bond OH \NH2 Table 1 (continued) Compound -R1 (-D-(cH)m-E-R4) _R2 -R3 I A Broken line -CHCH2CH(C2H5)2 /NH
336 1 -CH3 -C / 1 C Single bond NHCOOC(CH3)3 \NH2 -CHCH2C(CH 3)3 NH
337 ~ -CH3 _C 1 C Single bond NHSO2CH3 \NH2 NH
338 -CHCH2--C~ -CH3 -C// 1 C
NHSO2CH3 ~NH2 NH
339 -CH-~H -CH3 -C 1 C
NHCOOCH(CH3)2 \NH2 NH
340 -CHCH2 ~ A -CH3 _C 1 C
NHSO2CH3 ~NH2 NH
341 -CH2CH ~-~ -CH3 C 1 C
OCOOC2H5 \NH2 342 -CHCH2CH(C2H5)2 -CH3 C//NH 1 C
NHCOOC(CH3)3 \NH2 -C
I HCH2C(CH3)3 -CH3 CNH
NHSO2CH3 \NH2 344 -CHCH2C(CH3)3 -CH3 C//NH 1 C
OH \NH2 Table 1 (continued) Compound R1 (-D-(CH)m-E-R4' _R2 -R3 n A Broken line NH
345 -CI HCH2--C) -CH3 _C// 1 N
NHSO2CH3 \NH2 NH
346 -CH2CH ~~\ -CH3 C 1 N
NHCOOCH(CH3)2 NH2 NH
347 -CHCH2 ~ \ -CH3 C 1 N
NHSO2CH3 ~NH2 NH
348 -CH //\ -CH3 C 1 N
I _ OCOOC2H5 \NH2 349 -CHCH2C(CH3)3 -CH3 { CNH 1 N
NHSO2CH3 \NH2 350 -CHCH2CH(C2H5)2 -CH3 C~NH 1 N
NHCOOC(CH3)3 \NH ~
351 -CHCH2C(CH3)3 -CH3 C//NH 1 N
OH \NH2 NH
352 ~H -CH3 _C2 C Single bond NHSO2CH3 \NH2 NH
353 -CHCH2-(D -CH3 C 2 C Single bond NHCOOCH(CH3)2 \NH2 Table 1 (continued) Compound No. -R1 (D(CH)mER4) _R2 _R3 n A Brok en line CHCH2 r\ NH
354 -CH3 C~~ 2 C Single bond NHSO2CH3 \NH2 NH
355 C I _H2CH ~~ CH3 C//
2 C Single bond -CHCH2C(CH3)3 // NH
356 I -CH3 -C 2 C Single bond NHSO2CH3 \NH2 -CH(CH2)4CH3 /NH
357 ~ -CH3 _C ~ 2 C Single bond NHCOOC(CH3)3 \NH2 NH
358 -CHCH2CH(CH3)2 -CH3 C// 2 C Single bond OH \NH2 NH
NHSO2CH3 \NH2 ~--~ NH
360 -CHCH2-{ H -CH3 ? 2 C
~ ~ -C
NHCOOC2H5 \NH2 NH
361 -CHCH2-~) -CH3 -C2 C
I
NH
362 -CH2CH ~ ~ -CH3 C// 2 C
OCOOCH(CH3)2 \NH2 Table 1 (continued) Compound D-(CH)m-E-R4 2 3 No. -R1 R5 -R -R n A Broken line 363 -CHCH2C(CH3)3 -CH3 //NH
NHSO2CH3 \NH2 364 -CHC(SCH3)(CH3)2 -CH3 -C//NH 2 C
NHCOOC(CH3)3 ~NH2 365 -CHCH2CH(CH3)3 -CH3 C//NH 2 C
NH2 \NH2 NH
366 -CHCH2-CH~ -CH3 -C// 2 N
I
NHCOOC2H5 ~NH2 NH
367 -CHCH2--O -CH3 _C// 2 N
NHSO2CH3 ~NH2 NH
NHSO2CH3 ~NH2 - ~, NH
369 -CHCH2 r\~ COOH -CH3 C// 2 N
OCOOCH(CH3)2 ~NH2 -CHCH2C(CH3)i /NH/
370 CH3 , -C
\NH2 -CH(CH2)2SCH3 //NH
NHCOOC(CH3)3 \NH2 372 -CH2CH(CH2)3CH3 -CH3 ~NH 2 N
I -C
21~U~98 Table 1 (continued) Compound -D-(CH)m-E-R4 No. -R1 I -R2 -R3 n A Broken line NOH
373 /\ -H -C// 1 C Single bond \NH2 NOH
374 -CH2 / -H -C// 1 C Single bond \NH2 NOH
375 -CH2 - -H -C// 1 C Single bond \ /_ \NH2 376 -CH2_~\ -H -C // NOH 1 C Single bond ~ / \NH2 NOH
377 -CH2 /\ -H -C// 1 C Single bond S \NH2 378 -CH O-\ -H -C 1 C Single bond 2 \NH2 NOH
379 -CH2OCH2 /\ COOH -H -C// 1 C Single bond \NH2 ---NOH
380 -CH2SC2H5 -H -C// 1 C Single bond \NH2 NOH
381 -(CH2)4COOH -H -C// 1 C Single bond \NH2 \ NOH
382 -CHCH2 / -H C// 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Compound -D-(CH)m-E-R4 2 3 No. -R~ I 5 -R -R n A Broken line R
~\ NOH
383 -CHCH2 -'~, -H C// 1 C Single bond OH ~NH2 NOH
384 -CHCH2{~ -H C//
1 C Single bond NOH
385 -CHCH2 -H C1 C Single bond OCOOCH(CH3)2 NH2 ~ NOH
386 -CH2CH F_H _C// 1 C Single bond NHCHO \NH2 387 -CHCHZ-(' ~ -H NOH
I C 1 C Single bond NHCOOC2H5. NH2 NOH
388 -CHCH2 -H C// 1 C Single bond NHCOOCH(CH3)2 \NH2 NOH
389 -CHCH2 4_~> -H C// 1 C Single bond NHCOOC(CH;3)3 ~NH2 ~ ~\ NOH
390 -CHCH2~ -H C 1 C Single bond NH2 ~NH2 21~-0598 Table 1 (continued) Compound 1-D-(CH)m-E-R4 No. "R R2 -R3 n A Broken line NOH
391 -~H -H // 1 C Single bond OH \NH2 ~ NOH
392 -CHCH2-{ H) -H C// 1 C Single bond OCOCH3 ~--~ ~NH2 NOH
393 -CHCH2 4\ -H C// 1 C Single bond OCOOC2H5 \NH2 NOH
394 "CH-G) -H _C1 C Single bond NHCOOC2H5 \NH2 NOH
395 -CHCH2 n\ -H C1 C Single bond NHCOOCH(CH3)2 \NH2 NOH
396 "~H -H _C// 1 C Single bond NHCOOC(CH3)3 \NH2 NOH
397 -CHCH2_0 -H C 1 C Single bond NHCOOC(CH3)3 \NH2 NOH
398 -CH-G) -H _C 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Compound D-(CH)m-E-R4 No. -R1 I 5 -R2 R3 n A Broken line R
\ /NOH
399 -CHCH2 HI -H C/1 C Single bond NHSO2CH3 \NH
~
400 -CHCH2 H -H NOH -C1 C Single bond NH2 \NH2 NOH
1 C Single bond I -OH \NH2 NOH
402 CH -H -C~~ 1 C Single bond NH2 \NH2 403 -CH -H CNOH 1 C Single bond NHCOOC2H5 \NH2 404 -CH -H C// NOH 1 C Single bond NHCOOC(CH3)3 \NH2 -CHCH2CH(CH3)2 NOH
405 i -H -C~~ 1 C Single bond NHCOOC2H5 \NH2 -CHCH2CH(CH3)2 NOH
406 i -H _C~~ 1 C Single bond NHCOOC(CH3)3 \NHz -- -- I
-CHCH(CH3)2 /NOH
407 I -H _C ~ 1 C Single bond NHCOOC2H,, \NH2 Table 1 (continued) Compound -R1 D-(CH)m-E-Rq -R2 -R3 n A Broken line -CHCH(CH3)2 NOH
408 NHCOOC(CH3)3 -H -C 1 C Single bond \NH2 -CHC(CH3)3 /NOH
409 1 -H -C ~ 1 C Single bond NHCOOC2H5 \NH2 -CHC(CH3)3 /NOH
410 1 -H -C ~ 1 C Single bond NHCOOC(CH;3)3 \NH2 -CH(CH2)4CH3 /NOH
411 I -H -C ~ 1 C Single bond NHCOOC2H5 \NH2 CH(CH2)4CH3 NOH
412 I -H -C ~ 1 C Single bond NHCOOC(CH3)3 \NH2 413 I -H -C ~ 1 C Single bond NHCOOC2H5 \NH2 414 I -H C~ 1 C Single bond NHCOOC(CH3)3 \
-CH(CH2)4CH,3 /NOH
415 I -H -C ~ 1 C Single bond OCOOC2H5 \NH2 -CHCH2C(CH3)3 /NOH
416 I -H -C 1 C Single bond OCOOC2H5 \NH2 NOH
HCH2CH(C2H5)2 -H -C// 1 C Single bond I
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NOH
418 -H -C// 1 C Single bond NHCOOC2H5 \NH2 Table 1 (continued) Compound 1-D-(CH)m-E-R4 -R2 -R3 n A Broken line No. -R R5 -CHC(SCH3)(CH3)2 NOH
419 -H -C// 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 // NOH
420 I -H -C 1 C Single bond NHCOOCH(CH3)2 \NH2 -CHCH2C(CH3)3 /NOH
421 I -H -C ~ 1 C Single bond NH2 \NH2 ~
422 -CH--~H -H -C// NOH 1 C
OH \NH2 423 -CHCH2- { H~ -H C~NOH 1 C
OCOCH3 ~-- \NH2 424 -CHCH2--C> _H -C// NOH 1 C
OCOOC2H5 \NH2 ~ NOH
425 -CH-{ H ~ -H C 1 C
NH2 ~ ~ NH2 426 -CHCH2~ -H CNOH 1 C
NH2 \
~-~ ~NOH 427 CH-~ f{ ) -H C 1 C
~
373 /\ -H -C// 1 C Single bond \NH2 NOH
374 -CH2 / -H -C// 1 C Single bond \NH2 NOH
375 -CH2 - -H -C// 1 C Single bond \ /_ \NH2 376 -CH2_~\ -H -C // NOH 1 C Single bond ~ / \NH2 NOH
377 -CH2 /\ -H -C// 1 C Single bond S \NH2 378 -CH O-\ -H -C 1 C Single bond 2 \NH2 NOH
379 -CH2OCH2 /\ COOH -H -C// 1 C Single bond \NH2 ---NOH
380 -CH2SC2H5 -H -C// 1 C Single bond \NH2 NOH
381 -(CH2)4COOH -H -C// 1 C Single bond \NH2 \ NOH
382 -CHCH2 / -H C// 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Compound -D-(CH)m-E-R4 2 3 No. -R~ I 5 -R -R n A Broken line R
~\ NOH
383 -CHCH2 -'~, -H C// 1 C Single bond OH ~NH2 NOH
384 -CHCH2{~ -H C//
1 C Single bond NOH
385 -CHCH2 -H C1 C Single bond OCOOCH(CH3)2 NH2 ~ NOH
386 -CH2CH F_H _C// 1 C Single bond NHCHO \NH2 387 -CHCHZ-(' ~ -H NOH
I C 1 C Single bond NHCOOC2H5. NH2 NOH
388 -CHCH2 -H C// 1 C Single bond NHCOOCH(CH3)2 \NH2 NOH
389 -CHCH2 4_~> -H C// 1 C Single bond NHCOOC(CH;3)3 ~NH2 ~ ~\ NOH
390 -CHCH2~ -H C 1 C Single bond NH2 ~NH2 21~-0598 Table 1 (continued) Compound 1-D-(CH)m-E-R4 No. "R R2 -R3 n A Broken line NOH
391 -~H -H // 1 C Single bond OH \NH2 ~ NOH
392 -CHCH2-{ H) -H C// 1 C Single bond OCOCH3 ~--~ ~NH2 NOH
393 -CHCH2 4\ -H C// 1 C Single bond OCOOC2H5 \NH2 NOH
394 "CH-G) -H _C1 C Single bond NHCOOC2H5 \NH2 NOH
395 -CHCH2 n\ -H C1 C Single bond NHCOOCH(CH3)2 \NH2 NOH
396 "~H -H _C// 1 C Single bond NHCOOC(CH3)3 \NH2 NOH
397 -CHCH2_0 -H C 1 C Single bond NHCOOC(CH3)3 \NH2 NOH
398 -CH-G) -H _C 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Compound D-(CH)m-E-R4 No. -R1 I 5 -R2 R3 n A Broken line R
\ /NOH
399 -CHCH2 HI -H C/1 C Single bond NHSO2CH3 \NH
~
400 -CHCH2 H -H NOH -C1 C Single bond NH2 \NH2 NOH
1 C Single bond I -OH \NH2 NOH
402 CH -H -C~~ 1 C Single bond NH2 \NH2 403 -CH -H CNOH 1 C Single bond NHCOOC2H5 \NH2 404 -CH -H C// NOH 1 C Single bond NHCOOC(CH3)3 \NH2 -CHCH2CH(CH3)2 NOH
405 i -H -C~~ 1 C Single bond NHCOOC2H5 \NH2 -CHCH2CH(CH3)2 NOH
406 i -H _C~~ 1 C Single bond NHCOOC(CH3)3 \NHz -- -- I
-CHCH(CH3)2 /NOH
407 I -H _C ~ 1 C Single bond NHCOOC2H,, \NH2 Table 1 (continued) Compound -R1 D-(CH)m-E-Rq -R2 -R3 n A Broken line -CHCH(CH3)2 NOH
408 NHCOOC(CH3)3 -H -C 1 C Single bond \NH2 -CHC(CH3)3 /NOH
409 1 -H -C ~ 1 C Single bond NHCOOC2H5 \NH2 -CHC(CH3)3 /NOH
410 1 -H -C ~ 1 C Single bond NHCOOC(CH;3)3 \NH2 -CH(CH2)4CH3 /NOH
411 I -H -C ~ 1 C Single bond NHCOOC2H5 \NH2 CH(CH2)4CH3 NOH
412 I -H -C ~ 1 C Single bond NHCOOC(CH3)3 \NH2 413 I -H -C ~ 1 C Single bond NHCOOC2H5 \NH2 414 I -H C~ 1 C Single bond NHCOOC(CH3)3 \
-CH(CH2)4CH,3 /NOH
415 I -H -C ~ 1 C Single bond OCOOC2H5 \NH2 -CHCH2C(CH3)3 /NOH
416 I -H -C 1 C Single bond OCOOC2H5 \NH2 NOH
HCH2CH(C2H5)2 -H -C// 1 C Single bond I
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NOH
418 -H -C// 1 C Single bond NHCOOC2H5 \NH2 Table 1 (continued) Compound 1-D-(CH)m-E-R4 -R2 -R3 n A Broken line No. -R R5 -CHC(SCH3)(CH3)2 NOH
419 -H -C// 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 // NOH
420 I -H -C 1 C Single bond NHCOOCH(CH3)2 \NH2 -CHCH2C(CH3)3 /NOH
421 I -H -C ~ 1 C Single bond NH2 \NH2 ~
422 -CH--~H -H -C// NOH 1 C
OH \NH2 423 -CHCH2- { H~ -H C~NOH 1 C
OCOCH3 ~-- \NH2 424 -CHCH2--C> _H -C// NOH 1 C
OCOOC2H5 \NH2 ~ NOH
425 -CH-{ H ~ -H C 1 C
NH2 ~ ~ NH2 426 -CHCH2~ -H CNOH 1 C
NH2 \
~-~ ~NOH 427 CH-~ f{ ) -H C 1 C
~
~t4a598 Table 1 (continued) Compound R1 -D-(CH)m-E-R4 -R2 -R3 n A Broken line No. R5 NOH
428 -CHCH2--C ~ -H C~~ 1 C
NHCOOC2H5 \NH2 NOH
NHCOOCH(CH3)2 \NH2 NOH
430 -CH-~ -H -C 1 C
NHCOOCH(CH3)2 \NH2 NOH
431 -CHCH2-~H -H -C1 C
NHCOOCH(CH3)2 \NH2 NOH
-C
NHCOOC(CH,203 ~NH2 - -~ NOH
NHCOOC(CH3)3 ~NH2 -~-~- I
NHCOOC(CH3)3 \NH2 NOH
435 -CHCH2-G) -H -C 1 C
NHCOOC(CH3)3 ~NH2 Table 1 (continued) Co ~poound -Ri (-D-(CH)m-E-R4 -R2 -R3 n A Broken line NOH
NHCOOCH2 //i~\ ~NH2 NOH
NHSO2CH3 \NH2 NOH
NHSO2CH3 \NH2 NOH
439 -CHCH2-H~ -H -C// 1 C
NHSO2CH3 \NH2 440 -CH - o -H -C // NOH 1 C
NHS02in NH2 F-~---~
441 -CHCH2-{ H~ -H -C// NOH 1 C
NHSO2- ~--~ \) \NH2 `-~- +~- - -T-CNOH
442 -CHCHZ -~H -H
NHSO2CH2COOH ~NH2 NOH
I
OH \NH2 Table 1 (continued) Compound 1-(D(CH)mER4) -R2 -R3 n A Broken line No. "R R5 CHCH24-) NOH
NH2 \NH2 445 -CH2CH r-\ _ -H C ~NOH 1 C
OCOCH3 \NH2 NOH
446 -CHCH2 0\ -H C1 C
OCOOC2H5 \NH2 NOH
NHCOOC2H5 \NH2 NOH
NHCOOCH(CH3)2 \NH2 NOH
NHCOOC(CH~3)3 \NH2 NHCOOCH2 \NH2 _ -NOH
451 -CH2CH e--~ -H C// 1 C
NHSO2CH3 \NH2 Table 1 (continued) Com vpoound -R1 (-D-(cH)m-E-R4) -R2 -R3 n A Broken line / ~ NOH
NHSO2CH3 \NH2 453 -CH(CH2)4CH3 -H C// NOH 1 C
OH \NH2 454 -CHCH2C(CH3)3 H C// NOH 1 C
OH \NH2 -CHCH2CH(C2H5)2 // NOH
OCOCH3 \NH2 -CHCH2C(CH3)3 /NOH
456 I -H -C ~ 1 C
OCOOC2H5 \NH2 457 -CH2CH(CH2)2CH3 H // NOH 1 C
I -C
NHCHO
~NH2 -CHCH2C(CH3)3 NOH
458 _C
-CH(CH2)4CH3 NOH
NHCOOC2H,; ~NH2 -CHCH2CH(C2H5)2 NOH
NHCOOC2H5 ~NH2 CHCH2C(CH3)3 -H NOH
461 -H _C 1 C
NHCOOC2H5 \NH2 2140"398 Table 1 (continued) Compound R1 (D(cH)mER4) _R2 -R3 n A Broken line -CH(CH2)4CH3 NOH
462 1 -H _C 1 C
NHCOOCH(CH3)2 ~NH2 -CHCH2CH(C2H5)2 NOH
NHCOOCH(CH3)2 ~NH2 464 -CHCH2C(CH3)3 -H C~NOH 1 C
NHCOOCH(CH3)2 \NH2 -CH(CH2)4CH3 / NOH
465 1 -H _C / 1 C
NHCOOC(CH3)3 \NH2 NOH
466 -CHCH2CH(C2H5)2 -H C// 1 C
NHCOOC(CH3)3 \NH2 -CHCH2C(CH3)3 -H C// NOH
NHCOOC(CHs)3 ~NH2 -CH(CH2)2SCH3 ~NOH
468 1 -H _C 1 C
NHCOOC(CH3)3 ~NH2 -CHCH2C(CH3)3 NOH
\NH2 -CHCH2C(CH3)3 NOH
470 ~ -H _C 1 C
CH //NOH
471 i ~ -H _C 1 C
NHCOOC2H5 ~NH2 Table 1 (continued) Comvpoound R1 (DH)mER4) -R2 -R3 n A Broken line NOH
472 -CH / \ -H C// 1 C
NHCOOC(CH3)3 \NH2 -CHCH2CH(CH3)2 /NOH
NHCOOC2H5 ~NH2 -CHCH2CH(CH3)2 -H C // NOH
NHCOOC(CH3)3 \NH2 475 -CH(CH2)2CH3 H C// NOH 1 C
NHCOOCH(CH3)2 \NH2 NOH
476 -CH(CH2)2CH3 -H _C 1 C
NHCOOC(CH3)3 \NH2 -CHCH(CH3)2 //NOH
NHCOOCH(CH3)2 \NH2 -CHCH(CH3)2 // NOH
I ~
NHCOOC(CH3)3 \NH2 -CHC(CH3)3 //NOH
NHCOOCH(CH3)2 \NH2 NOH
480 -CHC(CH3)3 -H C// 1 C
NHCOOC(CH3)3 \NH2 481 -CHCH2Si(CH3)3 -H C// NOH 1 C
NHCOOC2H5 \NH2 Table 1 (continued) Comvpoound R1 (-D-(GH)m-E-R4) -R2 -R3 n A Broken line 482 -CHCH2Si(CH3)3 -H ~NOH C 1 C
NHCOOCH(CH3)2 \NH2 NHCOOC2H5 \NH2 NHCOOCH(CH3)2 \NH2 -CHCH2OC(CH3)3 // NOH
NHCOOC2H5 ~NH2 486 -CHCH2OC(CH3;)3 -H C~NOH 1 C
NHCOOCH(CH3)2 \NH2 487 -CHCH2OC(CH3)2C2H5 -H C// NOH 1 C
488 -CHCH2OC(CH3)2C2H5 -H
NHCOOCH(CH3)2 \NH2 489 -CHCH20C(C2H5)2CH3 -H -C // NOH
NHCOOC2H5 \NH2 490 -CHCH2OC(C2H5)2CH3 -H C// NOH 1 C
NHCOOCH(CH3)2 \NH2 491 -CHCH2OC(CH3)2CH(CH3)2 -H C// NOH 1 C
NHCOOCH(CH3)2 \NH2 492 -CHCH2SC(CH3)3 -H ~
NHCOOC2H5 \NH2 _ 2140598 Table 1 (continued) Compoound R~ D-(CH)m-E-R4 -R2 -R3 n A Broken line 493 -CHCH2SC(CH3)2C2H5 -H NOH C 1 C
NHCOOC2H5 \NH2 494 -CHCH2SC(CH3)2C2H5 -H C// NOH 1 C
NHCOOCH(CH3)2 \NH2 -CHC(CH3)2SC2H5 /NOH~
NHCOOC2H5 \NH2 496 -CHC(CH3)2SC2H5 -H C// NOH 1 C
NHCOOCH(CH3)2 I NH2 497 -CHC(CH3)2SCH(CH3)2 -H C// NOH 1 C
NHCOOC2H5 \NH2 -CHC(CH3)2SCH(CH3)2 /NOH
498 i H -C 1 C
NHCOOCH(CH3)2 \NH2 499 -CHC(CH3)2SCH(C2H5)2 NOH C
NHCOOC2H5 \NH2 -CHC(CH3)2SCH(C2H5)2 /NOH
NHCOOCH(CH3)2 NH2 501 -CH(CH2)4CH3 H C// NOH 1 C
NHSO2CH3 \NH2 502 -CHCH2C(CH3)3 -H C// NOH 1 C
NHSO2CH3 \NH2 z14o598 Table 1 (continued) Comvpo und R1 -D-(CH)m-E-R4 _R2 -R3 n A Broken line -CHCH2CH(C2H5)2 NOH
NHS02 ~~
\NH2 -CHCH2C(CH3)3 NOH
\NH2 NOH
505 -CH-<~ -H C 1 N
NHCOOCH(CH3)2 \NH2 NOH
506 -CHCH2- o H C// 1 N
NHCOOC2H5 \NH2 ~ NOH
507 -CH2CH ~_ ` -H C 1 N
NH2 ~NH2 NOH
508 -CHCH2 r,~, -H C// 1 N
NHCOOC(CH3)3 \NH2 509 -CHCH2C(CH3)3 -H /NOH 1 NF
C
NHCOOC2H5 \NH2 -CH(CH2)2SCH3 NOH
NHSO2CH3 ~NH2 NOH
511 -CHCH2 ~ -CH3 -C 2 C Single bond NHCOOCH(CH3)2 ~NH2 Table 1 (continued) Compound -R1 D-(CH)m-E-R4 -R2 -R3 n A Broken line ~-~ NOH
512 -CHCH2 -CH3 C// 2 C Single bond NHCOOC(CH3)3 \NH2 NOH
513 -CHCH2C(CH3)3 -CH3 C// 2 C Single bond NHCOOCH(CH3)2 \NH2 -CHCH2C(CH3)3 /NOH
514 I -CH3 _C ~ 2 C Single bond NHCOOC(CH3)3 \NH2 515 CH ~ H,-C ~~ 1 C Single bond NHCOOC(CH3)3 ~NHZ
516 -CHCH2 -~ -H _C// 1 C Single bond NHCOOCH(CH3)2 \NH2 517 -CHCH2- -H -oi/ 1 C Single bond OH \NH2 518 -CHCH2 -H _C// 1 C Single bond NHCOOC2H5 \NHZ
519 -CHCH2 ~- -H _c// 1 C Single bond NHSO2CH3 \NH2 520 -CH ~_ -H _C// 1 C Single bond OH \NHz Table 1 (continued) Compound -R1 (D(GH)mER4) _R2 -R3 n A Broken line -CHCH2C(CH,3)3 /NOCOOCH3 521 1 -H _C ~ 1 C Single bond NHCOOC2H5 ~NHZ
522 ~ 2( 3)3 -H -C~~ 1 C Single bond NHCOOCH(CH3)2 \NH2 -CHCH2C(CH3)3 /NOCOOCH3 523 ~ -H _~ 1 C Single bond NHCOOC(CH3)3 \NH2 -CHCH2C(CH3)3 //NOCOOCH3 524 i -H _~ 1 C Single bond OH \NH2 525 -CH -{ H } -H _C! 1 C
NHCOOC(CH3)3 \NH2 526 -CHCH2-H c// NOCOOCH3 1 C
NHCOOCH(CH3)2 \NHz 527 -CH-O -H _C// 1 C
OH \NHZ
~ ~ ~NOCOOCH3 528 -CHCH2-- -H ~ / 1 C
NHCOOC2H5 \NH2 529 -CHCH2 -H _C// 1 C
NHSO2CH3 \NH2 Table 1 (continued) Comvpoound -R1 -D-(CH)R,-E-R4 _R2 R3 n A Broken line 530 -CH -H _o// NOCOOCH3 1 C
OH \NH2 -CHCH2C(CH3)3 //ryvCOOCH3 531 I -H _C 1 C
NHCOOC2H5 \NHZ
-CHCH2C(CH3)3 /NOCOOCH3 532 1 -H _C ~ 1 C
NHCOOCH(CH3)2 \NHZ
533 -CHCH2C(CH3)3 -H C// NOCOOCH3 1 C
NHCOOC(CH3)3 \NH2 534 -CHCH2C(CH j)3 -H // NOCOOCH3 1 C
I C
OH \NH2 535 -CH-{H) -H -C// NOCOOCH3 1 C
NHCOOC2H5 \NH2 536 -CH -G) -H o// NOCOOCH3 1 C
NHCOOCH(CH3)2 \NHZ
537 -CHCH2--C -H _o// NOCOOCH3 1 C
NHCOOC2H5 \NH2 538 -CHCH2 -H _C// NOCOOCH3 1 C
NHCOOC(CH3)3 \NHZ
428 -CHCH2--C ~ -H C~~ 1 C
NHCOOC2H5 \NH2 NOH
NHCOOCH(CH3)2 \NH2 NOH
430 -CH-~ -H -C 1 C
NHCOOCH(CH3)2 \NH2 NOH
431 -CHCH2-~H -H -C1 C
NHCOOCH(CH3)2 \NH2 NOH
-C
NHCOOC(CH,203 ~NH2 - -~ NOH
NHCOOC(CH3)3 ~NH2 -~-~- I
NHCOOC(CH3)3 \NH2 NOH
435 -CHCH2-G) -H -C 1 C
NHCOOC(CH3)3 ~NH2 Table 1 (continued) Co ~poound -Ri (-D-(CH)m-E-R4 -R2 -R3 n A Broken line NOH
NHCOOCH2 //i~\ ~NH2 NOH
NHSO2CH3 \NH2 NOH
NHSO2CH3 \NH2 NOH
439 -CHCH2-H~ -H -C// 1 C
NHSO2CH3 \NH2 440 -CH - o -H -C // NOH 1 C
NHS02in NH2 F-~---~
441 -CHCH2-{ H~ -H -C// NOH 1 C
NHSO2- ~--~ \) \NH2 `-~- +~- - -T-CNOH
442 -CHCHZ -~H -H
NHSO2CH2COOH ~NH2 NOH
I
OH \NH2 Table 1 (continued) Compound 1-(D(CH)mER4) -R2 -R3 n A Broken line No. "R R5 CHCH24-) NOH
NH2 \NH2 445 -CH2CH r-\ _ -H C ~NOH 1 C
OCOCH3 \NH2 NOH
446 -CHCH2 0\ -H C1 C
OCOOC2H5 \NH2 NOH
NHCOOC2H5 \NH2 NOH
NHCOOCH(CH3)2 \NH2 NOH
NHCOOC(CH~3)3 \NH2 NHCOOCH2 \NH2 _ -NOH
451 -CH2CH e--~ -H C// 1 C
NHSO2CH3 \NH2 Table 1 (continued) Com vpoound -R1 (-D-(cH)m-E-R4) -R2 -R3 n A Broken line / ~ NOH
NHSO2CH3 \NH2 453 -CH(CH2)4CH3 -H C// NOH 1 C
OH \NH2 454 -CHCH2C(CH3)3 H C// NOH 1 C
OH \NH2 -CHCH2CH(C2H5)2 // NOH
OCOCH3 \NH2 -CHCH2C(CH3)3 /NOH
456 I -H -C ~ 1 C
OCOOC2H5 \NH2 457 -CH2CH(CH2)2CH3 H // NOH 1 C
I -C
NHCHO
~NH2 -CHCH2C(CH3)3 NOH
458 _C
-CH(CH2)4CH3 NOH
NHCOOC2H,; ~NH2 -CHCH2CH(C2H5)2 NOH
NHCOOC2H5 ~NH2 CHCH2C(CH3)3 -H NOH
461 -H _C 1 C
NHCOOC2H5 \NH2 2140"398 Table 1 (continued) Compound R1 (D(cH)mER4) _R2 -R3 n A Broken line -CH(CH2)4CH3 NOH
462 1 -H _C 1 C
NHCOOCH(CH3)2 ~NH2 -CHCH2CH(C2H5)2 NOH
NHCOOCH(CH3)2 ~NH2 464 -CHCH2C(CH3)3 -H C~NOH 1 C
NHCOOCH(CH3)2 \NH2 -CH(CH2)4CH3 / NOH
465 1 -H _C / 1 C
NHCOOC(CH3)3 \NH2 NOH
466 -CHCH2CH(C2H5)2 -H C// 1 C
NHCOOC(CH3)3 \NH2 -CHCH2C(CH3)3 -H C// NOH
NHCOOC(CHs)3 ~NH2 -CH(CH2)2SCH3 ~NOH
468 1 -H _C 1 C
NHCOOC(CH3)3 ~NH2 -CHCH2C(CH3)3 NOH
\NH2 -CHCH2C(CH3)3 NOH
470 ~ -H _C 1 C
CH //NOH
471 i ~ -H _C 1 C
NHCOOC2H5 ~NH2 Table 1 (continued) Comvpoound R1 (DH)mER4) -R2 -R3 n A Broken line NOH
472 -CH / \ -H C// 1 C
NHCOOC(CH3)3 \NH2 -CHCH2CH(CH3)2 /NOH
NHCOOC2H5 ~NH2 -CHCH2CH(CH3)2 -H C // NOH
NHCOOC(CH3)3 \NH2 475 -CH(CH2)2CH3 H C// NOH 1 C
NHCOOCH(CH3)2 \NH2 NOH
476 -CH(CH2)2CH3 -H _C 1 C
NHCOOC(CH3)3 \NH2 -CHCH(CH3)2 //NOH
NHCOOCH(CH3)2 \NH2 -CHCH(CH3)2 // NOH
I ~
NHCOOC(CH3)3 \NH2 -CHC(CH3)3 //NOH
NHCOOCH(CH3)2 \NH2 NOH
480 -CHC(CH3)3 -H C// 1 C
NHCOOC(CH3)3 \NH2 481 -CHCH2Si(CH3)3 -H C// NOH 1 C
NHCOOC2H5 \NH2 Table 1 (continued) Comvpoound R1 (-D-(GH)m-E-R4) -R2 -R3 n A Broken line 482 -CHCH2Si(CH3)3 -H ~NOH C 1 C
NHCOOCH(CH3)2 \NH2 NHCOOC2H5 \NH2 NHCOOCH(CH3)2 \NH2 -CHCH2OC(CH3)3 // NOH
NHCOOC2H5 ~NH2 486 -CHCH2OC(CH3;)3 -H C~NOH 1 C
NHCOOCH(CH3)2 \NH2 487 -CHCH2OC(CH3)2C2H5 -H C// NOH 1 C
488 -CHCH2OC(CH3)2C2H5 -H
NHCOOCH(CH3)2 \NH2 489 -CHCH20C(C2H5)2CH3 -H -C // NOH
NHCOOC2H5 \NH2 490 -CHCH2OC(C2H5)2CH3 -H C// NOH 1 C
NHCOOCH(CH3)2 \NH2 491 -CHCH2OC(CH3)2CH(CH3)2 -H C// NOH 1 C
NHCOOCH(CH3)2 \NH2 492 -CHCH2SC(CH3)3 -H ~
NHCOOC2H5 \NH2 _ 2140598 Table 1 (continued) Compoound R~ D-(CH)m-E-R4 -R2 -R3 n A Broken line 493 -CHCH2SC(CH3)2C2H5 -H NOH C 1 C
NHCOOC2H5 \NH2 494 -CHCH2SC(CH3)2C2H5 -H C// NOH 1 C
NHCOOCH(CH3)2 \NH2 -CHC(CH3)2SC2H5 /NOH~
NHCOOC2H5 \NH2 496 -CHC(CH3)2SC2H5 -H C// NOH 1 C
NHCOOCH(CH3)2 I NH2 497 -CHC(CH3)2SCH(CH3)2 -H C// NOH 1 C
NHCOOC2H5 \NH2 -CHC(CH3)2SCH(CH3)2 /NOH
498 i H -C 1 C
NHCOOCH(CH3)2 \NH2 499 -CHC(CH3)2SCH(C2H5)2 NOH C
NHCOOC2H5 \NH2 -CHC(CH3)2SCH(C2H5)2 /NOH
NHCOOCH(CH3)2 NH2 501 -CH(CH2)4CH3 H C// NOH 1 C
NHSO2CH3 \NH2 502 -CHCH2C(CH3)3 -H C// NOH 1 C
NHSO2CH3 \NH2 z14o598 Table 1 (continued) Comvpo und R1 -D-(CH)m-E-R4 _R2 -R3 n A Broken line -CHCH2CH(C2H5)2 NOH
NHS02 ~~
\NH2 -CHCH2C(CH3)3 NOH
\NH2 NOH
505 -CH-<~ -H C 1 N
NHCOOCH(CH3)2 \NH2 NOH
506 -CHCH2- o H C// 1 N
NHCOOC2H5 \NH2 ~ NOH
507 -CH2CH ~_ ` -H C 1 N
NH2 ~NH2 NOH
508 -CHCH2 r,~, -H C// 1 N
NHCOOC(CH3)3 \NH2 509 -CHCH2C(CH3)3 -H /NOH 1 NF
C
NHCOOC2H5 \NH2 -CH(CH2)2SCH3 NOH
NHSO2CH3 ~NH2 NOH
511 -CHCH2 ~ -CH3 -C 2 C Single bond NHCOOCH(CH3)2 ~NH2 Table 1 (continued) Compound -R1 D-(CH)m-E-R4 -R2 -R3 n A Broken line ~-~ NOH
512 -CHCH2 -CH3 C// 2 C Single bond NHCOOC(CH3)3 \NH2 NOH
513 -CHCH2C(CH3)3 -CH3 C// 2 C Single bond NHCOOCH(CH3)2 \NH2 -CHCH2C(CH3)3 /NOH
514 I -CH3 _C ~ 2 C Single bond NHCOOC(CH3)3 \NH2 515 CH ~ H,-C ~~ 1 C Single bond NHCOOC(CH3)3 ~NHZ
516 -CHCH2 -~ -H _C// 1 C Single bond NHCOOCH(CH3)2 \NH2 517 -CHCH2- -H -oi/ 1 C Single bond OH \NH2 518 -CHCH2 -H _C// 1 C Single bond NHCOOC2H5 \NHZ
519 -CHCH2 ~- -H _c// 1 C Single bond NHSO2CH3 \NH2 520 -CH ~_ -H _C// 1 C Single bond OH \NHz Table 1 (continued) Compound -R1 (D(GH)mER4) _R2 -R3 n A Broken line -CHCH2C(CH,3)3 /NOCOOCH3 521 1 -H _C ~ 1 C Single bond NHCOOC2H5 ~NHZ
522 ~ 2( 3)3 -H -C~~ 1 C Single bond NHCOOCH(CH3)2 \NH2 -CHCH2C(CH3)3 /NOCOOCH3 523 ~ -H _~ 1 C Single bond NHCOOC(CH3)3 \NH2 -CHCH2C(CH3)3 //NOCOOCH3 524 i -H _~ 1 C Single bond OH \NH2 525 -CH -{ H } -H _C! 1 C
NHCOOC(CH3)3 \NH2 526 -CHCH2-H c// NOCOOCH3 1 C
NHCOOCH(CH3)2 \NHz 527 -CH-O -H _C// 1 C
OH \NHZ
~ ~ ~NOCOOCH3 528 -CHCH2-- -H ~ / 1 C
NHCOOC2H5 \NH2 529 -CHCH2 -H _C// 1 C
NHSO2CH3 \NH2 Table 1 (continued) Comvpoound -R1 -D-(CH)R,-E-R4 _R2 R3 n A Broken line 530 -CH -H _o// NOCOOCH3 1 C
OH \NH2 -CHCH2C(CH3)3 //ryvCOOCH3 531 I -H _C 1 C
NHCOOC2H5 \NHZ
-CHCH2C(CH3)3 /NOCOOCH3 532 1 -H _C ~ 1 C
NHCOOCH(CH3)2 \NHZ
533 -CHCH2C(CH3)3 -H C// NOCOOCH3 1 C
NHCOOC(CH3)3 \NH2 534 -CHCH2C(CH j)3 -H // NOCOOCH3 1 C
I C
OH \NH2 535 -CH-{H) -H -C// NOCOOCH3 1 C
NHCOOC2H5 \NH2 536 -CH -G) -H o// NOCOOCH3 1 C
NHCOOCH(CH3)2 \NHZ
537 -CHCH2--C -H _o// NOCOOCH3 1 C
NHCOOC2H5 \NH2 538 -CHCH2 -H _C// NOCOOCH3 1 C
NHCOOC(CH3)3 \NHZ
z14o59s Table 1 (continued) Compound -R1 -D-(CH)m-E-R4 -R2 -R3 n A Broken line 539 -CHCH2CH(CH3)2 -H NOCOOCH3 1 c C
NHCOOC2H5 \NHz -CHCH2CH(CH3)2 -H c// NOCOOCH3 1 C
NHCOOCH(CH3)2 \NH2 541 "CH ~ -H ~~~ 1 C Single bond NHCOOC(CH,03 NHz 542 -CHCH2--~ -H _C// 1 C Single bond NHCOOCH(CH3)2 \NHZ
543 -CH - o -H -C // 1 C Single bond OH \NH2 NOCOOCZHS
544 -CHCH2 -H _C// 1 C Single bond I
NHCOOC2H5 ~NHZ
545 -CHCH2 ~, -H 1 C Single bond I
NHSO2CH3 ~NHZ
NOCOOCZHS
546 -CH /-H C 1 C Single bond OH \NH2 HCH2C(CH3)3 // NOCOOC2H5 547 ~ -H _~ 1 C Single bond NHCOOCH(CH3)2 \NH2 Table 1 (continued) Co npoound -R1 (D(GH)mER4) -R2 -R3 n A Broken line -CHCH2C(CH3)3 // NOCOOC2H5 548 ~ -H ~ 1 C Single bond OH \NH2 549 -CH -(~) -H _C// NOCOOCZHS 1 C
NHCOOC(CH3)3 \NH2 550 -CHCH2--~ -H _o~~ NOCOOC2H5 1 C
NHCOOCH(CH3)2 \NH2 NOCOOCzHs C
OH \NH2 552 -CHCH2 4~\ -H // NOCOOC2H5 1 C
C
NHCOOC2H5 \NH2 NOCOOCZHS
553 -CHCH2- n\ H C 1 C
- --r--~ ~
~
_ OH \NH2 555 -CHCH2C(CH3)3 -H CNOCOOCzHs 1 C
NHCOOCH(CH3)2 \NHz T-C
556 -CHCH2C(CH3)3 -H NOCOOC2H5 1 C
OH \NH2 .214059S
Table 1 (continued) Comvpoound R~ (D(CH)mER4) -R2 -R3 n A Broken line R' NHCOOC(CH3)3 \NH2 NHCOOC2H5 \NH2 ~
, 559 -CH -(~) -H -c 1 C
NHCOOCH(CH3)2 NH2 560 "CH -G) -H c// NOCOOC2H5 1 C
NHCOOC2H5 \NHZ
561 -CHCH2C(CH3)3 -H // NOCOOC2H5 1 C
I C
NHCOOC2H5 \NH2 562 -CHCH2C(CH3)3 -H C// NOCOOC2H5 1 C
NHCOOC(CH3)3 \NH2 563 -CHCH2C(CH3)2 -H CNOCOOCzHs 1 C
OCOOC2H5 \NH2 564 -CHCH2CH(CH3)2 -H C// NOCOOC2H5 1 C
NHCOOCH(CH3)2 \NHZ
565 CHCH2-H -C// 1 C Single bond NHCOOC(CH3)3 \NH2 214U5"98 Table 1 (continued) Comvpoound R1 (D(CH)mER4 -R2 -R3 n A Broken line 566 -CHCH2-{> -H _C1 C Single bond NHSO2CH3 \NH2 567 -~H~ -H _C// 1 C Single bond OH \NH2 ~ ~ /NCH3 568 -CHCH2- -H -C ~ 1 C Single bond NHSO2CH3 \NH2 569 -CHCH2C(CH3)3 -H C// 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)g // NCH3 570 I -H -C 1 C Single bond NHSO2CH3 \NH2 571 -CHCH2-o -H _C// 1 C
NHCOOC(CH3)3 \NH2 572 -CHCH2-- H~ -H -C//
NHSO2CH3 \NH2 NCHg -H _C/
573 -CH -(~) 574 -CHCH2-~) -H C 1 C
NHSO2CH3 \NH2 Table 1 (continued) Compound _R1 -D-(CH)m-E-R4 R2 -R3 n A Broken line No. R5 -CHCH2C(CH3)3 -H NCH3 1 C
NHCOOC2H5 ~NH2 -CHCH2C(CH3)3 // NCH3 C
NHSO2CH3 ~NH2 577 -CHCH2- H~ -H -C 1 C Single bond NHCOOC(CH3)3 NH2 578 -CHCH2 -- < H -H _C 1 C Single bond 579 -CH -~H -H C 1 C Single bond OH ~ NH2 ~ ~ ~NCOCH3 580 CHCH2~ H C~ 1 C Single bond -CHCH2C(CH3)3 NCOCH3 581 -H -C 1 C Single bond 582 CHCH2C(CH3)3 NCOCH3 -H _C 1 C Single bond NHCOOC(CH3)3 ~NH2 Table 1 (continued) Compound R~ -D-(CH)m-E:-R4 -R2 -R3 n A Broken line No. R5 584 -CHCH2-~H> -H C// NCOCH3 1 C
NHSO2CH3 \NH2 585 -CH-~ -H -C// 1 C
OH \NH2 NHSO2CH3 \NH2 -CHCH2C(CH3)3 -H C// 1 C
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NCOCH3 NHSO2CH3 C\NH2 589 -CHCH2-~H -H C~ 1 C Single bond NHCOOC(CH3)3 \NH2 590 -CHCH2--~) -H _C 1 C Single bond NHSO2CH3 ~NH2 591 -CH - o -H -C ~ 1 C Single bond OH ~ NH2 592 -CHCH2 -H -C 1 C Single bond NHSO2CH3 \NH2 .___ Table 1 (continued) Compound -R1 -D-(CH)m-E-R4 -R2 -R3 n A Broken line NCOOCHg HCH2C(CH3)3 -H -C ~ 1 C Single bond I
NHCOOC2H5 \NH2 -CHCH2C(CH;3)3 /NCOOCH3 594 1 -H _C 1 C Single bond NHSO2CH3 \NH2 595 -CHCH2-C) -H //NCOOCH3 _C 1 C
NHCOOC(CH3)3 \NH2 596 -CHCH2-O -H _C// NCOOCH3 1 C
NHSO2CH3 \NH2 ~COOCH3 597 'CH ~ -H C 1 C
OH \NH2 598 -CHCH2 4\` -H _C// 1 C
NHSO2CH3 \NH2 599 -CHCH2C(CH3)3 -H NCOOCH3 1 C
NHCOOC2H5 C\NH
600 -CHCH2C(CH3)3 -H C// NCOOCH3 1 C
NHSO2CH3 \NH2 601 CHCH2-~H -H C// 1 C Single bond NHCOOC(CH3)3 NH2 '2140598 Table 1 (continued) Compound -R1 (D(CH)mER4" -R2 -R3 n A Broken line 602 -CHCH2-H> -H C// 1 C Single bond NHSO2CH3 ~NH2 603 -CH -H C// 1 C Single bond I
OH \NH2 604 -CHCH2 -H C// 1 C Single bond I
NHSO2CH3 \NH2 605 -CHCH2C(CHg)3 -H hC~/ 1 C Single bond NHCOOC2H5 \NH2 606 -CHCH2C(CH3)3 -H C// 1 C Single bond NHSO2CH3 \NH2 NHCOOC(CHS)3 \NH2 I
NHSO2CH3 \NH2 I
OH \NH2 NHSO2CH3 \NH2 Table 1 (continued) Compound (-D-(cH)m-E-R4 No. -R~ I 5 R2 -R3 n A Broken line R
611 -CHCH2C(CH3)3 -H C~NOCOCH3 1 C
I
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 /NOCOCH3 612 i -H C~ 1 C
NHSO2CH3 \NH2 ~---~ NOCH3 613 -CHCH2-{ H) -H -C// 1 C Single bond I ~--~
NHCOOC(CH3)3 \NH2 614 -CHCH2 H -H -C// 1 C Single bond NHSO2CH3 \NH2 615 '~H~ -H -C// 1 C Single bond OH \NH2 ~-~ NOCH3 616 C H C H 2 -H _C// 1 C Single bond NHSO2CH3 \NH2 -CHCH2C(CH3)3 ~ NOCH3 617 I -H -C 1 C Single bond NHCOOC2H5 \NH2 CHCH2C(CH3)3 OCH3 618 I ~H -C 1 C Single bond NHSO2CH3 \NH2 619 -CHCH2-{ -H ' 'I C
I ~--~ -C
NHCOOC(CH3)3 \NH2 .._ Table 1 (continued) Compound (D-(CH)mE-R4) No. -R1 ( -R2 -R3 n A Broken line ~-620 -CHCH2-{ H > -H -C// NOCH3 NHSO2CH~3- \NH2 621 -CH-(~) -H -C/
I OH \NH2 NHSO2CH3 \NH2 -CHCH2C(CH3)3 //NOCHg NHCOOC2H5 \NH2 -CHCH2C(CH3)3 /NOCH3/
NHSO2CH3 \NH2 -CHCH - ( N ) NOCOCH2OH
625 I 2 -H _C// 1 C Single bond NHCOOC(CH3)3 \NH2 ~ NOCOCHZOH
626 CHCH2 H -H C// 1 C Single bond ~
CH H -H _C// 1 C Single bond OH \NH2 628 CHCH2 -H NOCOCHzOH
C// 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Compound 1D-(CH)m-E-R4 -R2 -R3 n A Broken line No. -R R5 -CHCH2C(CH3)3 NOCOCH2OH
629 -H C// 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NOCOCH2OH
630 I -H _C// 1 C Single bond NHSO2CH3 \NHZ
631 -CHCH2--( H } //NOCOCHZOH
I ~/ -H -C 1 C
NHCOOC(CH3)3 \NH2 632 -CHCH2 H -H NOCOCH2OH 1 c c NHSO2CH3 \NH2 633 -CH H -H c 1 C
QH \NH2 634 -CHCH2 r_\~ /NOCOCH2OH 1 C
-H C
NHSO2CH3 \NH2 -CHCH2C(CH3)3 NOCOCH2OH
635 -H _C// 1 C
NHCOOC2H5 \NH2 636 -CHCH2C(CH3)3 -H C//NOCOCH2OH
NHSO2CH3 \NH2 NH
637 CHCH2-~H -H -NHC 1 C Single bond NHCOOC(CH3)3 \NH2 Table 1 (continued) Comvpoound -R1 -D-(CH)R,-E-R4 -R2 -R3 n A Broken line NH
638 -CHCH2- Ho -H -NHC 1 C Single bond NHSO2CH3 \NH2 NH
639 -CH -(D -H -NHC 1 C Single bond NH
640 -CHCH2 r\ -H -NHC // 1 C Single bond NHSO2CH3 \NH2 NH
641 -CHCH2C(CH3)3 -H -NHC// 1 C Single bond NHCOOC2H5 \NH2 NH
642 -CHCH2C(CH3)3 -H -NHC 1 C Single bond NHSO2CH3 \NH2 NH
643 -CHCH2-<~) -H -NHC// 1 C
NHCOOC(CH3)3 \NH2 NH
NHSO2CH3 ~NH2 NH
645 -CH <DH -H -NHC 1 C
NH
NHCOOC2H5 \NHz -CHCH2CH(CH3)2 -H c// NOCOOCH3 1 C
NHCOOCH(CH3)2 \NH2 541 "CH ~ -H ~~~ 1 C Single bond NHCOOC(CH,03 NHz 542 -CHCH2--~ -H _C// 1 C Single bond NHCOOCH(CH3)2 \NHZ
543 -CH - o -H -C // 1 C Single bond OH \NH2 NOCOOCZHS
544 -CHCH2 -H _C// 1 C Single bond I
NHCOOC2H5 ~NHZ
545 -CHCH2 ~, -H 1 C Single bond I
NHSO2CH3 ~NHZ
NOCOOCZHS
546 -CH /-H C 1 C Single bond OH \NH2 HCH2C(CH3)3 // NOCOOC2H5 547 ~ -H _~ 1 C Single bond NHCOOCH(CH3)2 \NH2 Table 1 (continued) Co npoound -R1 (D(GH)mER4) -R2 -R3 n A Broken line -CHCH2C(CH3)3 // NOCOOC2H5 548 ~ -H ~ 1 C Single bond OH \NH2 549 -CH -(~) -H _C// NOCOOCZHS 1 C
NHCOOC(CH3)3 \NH2 550 -CHCH2--~ -H _o~~ NOCOOC2H5 1 C
NHCOOCH(CH3)2 \NH2 NOCOOCzHs C
OH \NH2 552 -CHCH2 4~\ -H // NOCOOC2H5 1 C
C
NHCOOC2H5 \NH2 NOCOOCZHS
553 -CHCH2- n\ H C 1 C
- --r--~ ~
~
_ OH \NH2 555 -CHCH2C(CH3)3 -H CNOCOOCzHs 1 C
NHCOOCH(CH3)2 \NHz T-C
556 -CHCH2C(CH3)3 -H NOCOOC2H5 1 C
OH \NH2 .214059S
Table 1 (continued) Comvpoound R~ (D(CH)mER4) -R2 -R3 n A Broken line R' NHCOOC(CH3)3 \NH2 NHCOOC2H5 \NH2 ~
, 559 -CH -(~) -H -c 1 C
NHCOOCH(CH3)2 NH2 560 "CH -G) -H c// NOCOOC2H5 1 C
NHCOOC2H5 \NHZ
561 -CHCH2C(CH3)3 -H // NOCOOC2H5 1 C
I C
NHCOOC2H5 \NH2 562 -CHCH2C(CH3)3 -H C// NOCOOC2H5 1 C
NHCOOC(CH3)3 \NH2 563 -CHCH2C(CH3)2 -H CNOCOOCzHs 1 C
OCOOC2H5 \NH2 564 -CHCH2CH(CH3)2 -H C// NOCOOC2H5 1 C
NHCOOCH(CH3)2 \NHZ
565 CHCH2-H -C// 1 C Single bond NHCOOC(CH3)3 \NH2 214U5"98 Table 1 (continued) Comvpoound R1 (D(CH)mER4 -R2 -R3 n A Broken line 566 -CHCH2-{> -H _C1 C Single bond NHSO2CH3 \NH2 567 -~H~ -H _C// 1 C Single bond OH \NH2 ~ ~ /NCH3 568 -CHCH2- -H -C ~ 1 C Single bond NHSO2CH3 \NH2 569 -CHCH2C(CH3)3 -H C// 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)g // NCH3 570 I -H -C 1 C Single bond NHSO2CH3 \NH2 571 -CHCH2-o -H _C// 1 C
NHCOOC(CH3)3 \NH2 572 -CHCH2-- H~ -H -C//
NHSO2CH3 \NH2 NCHg -H _C/
573 -CH -(~) 574 -CHCH2-~) -H C 1 C
NHSO2CH3 \NH2 Table 1 (continued) Compound _R1 -D-(CH)m-E-R4 R2 -R3 n A Broken line No. R5 -CHCH2C(CH3)3 -H NCH3 1 C
NHCOOC2H5 ~NH2 -CHCH2C(CH3)3 // NCH3 C
NHSO2CH3 ~NH2 577 -CHCH2- H~ -H -C 1 C Single bond NHCOOC(CH3)3 NH2 578 -CHCH2 -- < H -H _C 1 C Single bond 579 -CH -~H -H C 1 C Single bond OH ~ NH2 ~ ~ ~NCOCH3 580 CHCH2~ H C~ 1 C Single bond -CHCH2C(CH3)3 NCOCH3 581 -H -C 1 C Single bond 582 CHCH2C(CH3)3 NCOCH3 -H _C 1 C Single bond NHCOOC(CH3)3 ~NH2 Table 1 (continued) Compound R~ -D-(CH)m-E:-R4 -R2 -R3 n A Broken line No. R5 584 -CHCH2-~H> -H C// NCOCH3 1 C
NHSO2CH3 \NH2 585 -CH-~ -H -C// 1 C
OH \NH2 NHSO2CH3 \NH2 -CHCH2C(CH3)3 -H C// 1 C
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NCOCH3 NHSO2CH3 C\NH2 589 -CHCH2-~H -H C~ 1 C Single bond NHCOOC(CH3)3 \NH2 590 -CHCH2--~) -H _C 1 C Single bond NHSO2CH3 ~NH2 591 -CH - o -H -C ~ 1 C Single bond OH ~ NH2 592 -CHCH2 -H -C 1 C Single bond NHSO2CH3 \NH2 .___ Table 1 (continued) Compound -R1 -D-(CH)m-E-R4 -R2 -R3 n A Broken line NCOOCHg HCH2C(CH3)3 -H -C ~ 1 C Single bond I
NHCOOC2H5 \NH2 -CHCH2C(CH;3)3 /NCOOCH3 594 1 -H _C 1 C Single bond NHSO2CH3 \NH2 595 -CHCH2-C) -H //NCOOCH3 _C 1 C
NHCOOC(CH3)3 \NH2 596 -CHCH2-O -H _C// NCOOCH3 1 C
NHSO2CH3 \NH2 ~COOCH3 597 'CH ~ -H C 1 C
OH \NH2 598 -CHCH2 4\` -H _C// 1 C
NHSO2CH3 \NH2 599 -CHCH2C(CH3)3 -H NCOOCH3 1 C
NHCOOC2H5 C\NH
600 -CHCH2C(CH3)3 -H C// NCOOCH3 1 C
NHSO2CH3 \NH2 601 CHCH2-~H -H C// 1 C Single bond NHCOOC(CH3)3 NH2 '2140598 Table 1 (continued) Compound -R1 (D(CH)mER4" -R2 -R3 n A Broken line 602 -CHCH2-H> -H C// 1 C Single bond NHSO2CH3 ~NH2 603 -CH -H C// 1 C Single bond I
OH \NH2 604 -CHCH2 -H C// 1 C Single bond I
NHSO2CH3 \NH2 605 -CHCH2C(CHg)3 -H hC~/ 1 C Single bond NHCOOC2H5 \NH2 606 -CHCH2C(CH3)3 -H C// 1 C Single bond NHSO2CH3 \NH2 NHCOOC(CHS)3 \NH2 I
NHSO2CH3 \NH2 I
OH \NH2 NHSO2CH3 \NH2 Table 1 (continued) Compound (-D-(cH)m-E-R4 No. -R~ I 5 R2 -R3 n A Broken line R
611 -CHCH2C(CH3)3 -H C~NOCOCH3 1 C
I
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 /NOCOCH3 612 i -H C~ 1 C
NHSO2CH3 \NH2 ~---~ NOCH3 613 -CHCH2-{ H) -H -C// 1 C Single bond I ~--~
NHCOOC(CH3)3 \NH2 614 -CHCH2 H -H -C// 1 C Single bond NHSO2CH3 \NH2 615 '~H~ -H -C// 1 C Single bond OH \NH2 ~-~ NOCH3 616 C H C H 2 -H _C// 1 C Single bond NHSO2CH3 \NH2 -CHCH2C(CH3)3 ~ NOCH3 617 I -H -C 1 C Single bond NHCOOC2H5 \NH2 CHCH2C(CH3)3 OCH3 618 I ~H -C 1 C Single bond NHSO2CH3 \NH2 619 -CHCH2-{ -H ' 'I C
I ~--~ -C
NHCOOC(CH3)3 \NH2 .._ Table 1 (continued) Compound (D-(CH)mE-R4) No. -R1 ( -R2 -R3 n A Broken line ~-620 -CHCH2-{ H > -H -C// NOCH3 NHSO2CH~3- \NH2 621 -CH-(~) -H -C/
I OH \NH2 NHSO2CH3 \NH2 -CHCH2C(CH3)3 //NOCHg NHCOOC2H5 \NH2 -CHCH2C(CH3)3 /NOCH3/
NHSO2CH3 \NH2 -CHCH - ( N ) NOCOCH2OH
625 I 2 -H _C// 1 C Single bond NHCOOC(CH3)3 \NH2 ~ NOCOCHZOH
626 CHCH2 H -H C// 1 C Single bond ~
CH H -H _C// 1 C Single bond OH \NH2 628 CHCH2 -H NOCOCHzOH
C// 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Compound 1D-(CH)m-E-R4 -R2 -R3 n A Broken line No. -R R5 -CHCH2C(CH3)3 NOCOCH2OH
629 -H C// 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NOCOCH2OH
630 I -H _C// 1 C Single bond NHSO2CH3 \NHZ
631 -CHCH2--( H } //NOCOCHZOH
I ~/ -H -C 1 C
NHCOOC(CH3)3 \NH2 632 -CHCH2 H -H NOCOCH2OH 1 c c NHSO2CH3 \NH2 633 -CH H -H c 1 C
QH \NH2 634 -CHCH2 r_\~ /NOCOCH2OH 1 C
-H C
NHSO2CH3 \NH2 -CHCH2C(CH3)3 NOCOCH2OH
635 -H _C// 1 C
NHCOOC2H5 \NH2 636 -CHCH2C(CH3)3 -H C//NOCOCH2OH
NHSO2CH3 \NH2 NH
637 CHCH2-~H -H -NHC 1 C Single bond NHCOOC(CH3)3 \NH2 Table 1 (continued) Comvpoound -R1 -D-(CH)R,-E-R4 -R2 -R3 n A Broken line NH
638 -CHCH2- Ho -H -NHC 1 C Single bond NHSO2CH3 \NH2 NH
639 -CH -(D -H -NHC 1 C Single bond NH
640 -CHCH2 r\ -H -NHC // 1 C Single bond NHSO2CH3 \NH2 NH
641 -CHCH2C(CH3)3 -H -NHC// 1 C Single bond NHCOOC2H5 \NH2 NH
642 -CHCH2C(CH3)3 -H -NHC 1 C Single bond NHSO2CH3 \NH2 NH
643 -CHCH2-<~) -H -NHC// 1 C
NHCOOC(CH3)3 \NH2 NH
NHSO2CH3 ~NH2 NH
645 -CH <DH -H -NHC 1 C
NH
_ Table 1 (continued) Compound R1 (D(CH)mER4' -R2 -R3 n A Broken line 647 -CHCH2C(CH3)3 -H NH 1 C
I -NHC
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 /NH
648 I -H -NHC ~ 1 C
NHSO2CH3 \NH2 649 -CHCH2--C) -H -NHC 1 C Single bond NHCOOC(CH33)3 \NH2 ----'r---650 -CHCH2--C) -H -NHC// 1 C Single bond NHSO2CH3 ~ NH2 651 -~H ~ -H NHC 1 C Single bond OH ~ NH2 652 -CHCH2-1c) -H -NHC 1 C Single bond I
NHSO2CH3 \NH2 - - -~-653 -CHCH2C(CH3)3 -H NHC// NCH3 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 // NCH3 654 1 -H -NHC 1 C Single bond NHSO2CH3 \NH2 655 -CHCH2-~H -H -NHC 1 C
NHCOOC(CH3)3 \NH2 c Table 1 (continued) Compound 1-D-(CH)m-E-R4 No. -R _R2 -R3 n A Broken line 656 -CHCH2--C NCHg I -NHC
NHSO2CH3 \NH2 OH ~ NH2 NHSO2CH3 \NH2 659 -CHCH2C(CH3)3 -H NHC// NCH3 NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NCH3 ~^--661 2-C' -H -NHC / 1 C Single bond NHCOOC(CH3)3 \NH2 662 CHCH2 H) H,, -NHC/i 1 C Single bond NHSO2CH3 \NHZ
~- -663 CH H -H NHC 1 C Single bond OH \NHz 664 -CHCH2 -H -NHC 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Compoound R1 (-D-(cH)m-E-R4) -R2 -R3 n A Broken line -CHCH2C(CH3)3 NCOCH
665 1 C Single bond -H _NHC % 3 NHCOOC2H5 \NHz -CHCH2C(CH3)3 NCOCH3 666 -H -NHC// 1 C Single bond NHSO2CH3 \NH2 NHCOOC(CH3)3 \NHZ
668 -CHCH2 H) -H -NHC NCOCH3 1 C
NHSO2CH3 ~NH2 669 -CH ~ -H -NHC// NCOCH3 1 C
Qm ~NH2 670 -CHCH2 r\ -H -NHCNCOCH3 1 C
NHSO2CH3 ~NH2 671 -CHCH2C(CH3)3 -H NCOCH3 1 C
672 -CHCH2C(CH3)3 -H NCOCH3 1 C
-NHC
NHSO2CH3 \NH2 673 -CHCH2 -H -NHC// 1 C Single bond NHCOOC(CH3)3 \NHz Table 1 (continued) Compound 1-D-(CH)m-E-R4 -R2 -R3 n A Broken line No. -R R5 ~~ NOCOCH3 674 -CHCH2-( H> -H -NHC// 1 C Single bond NHSO2CH3~ NHZ
675 -CH ~ -H -NHC// 1 C Single bond OH \NH2 CHCH OcoCH3 676 I 2~ -H ,-NHC 1 C Single bond NHSO2CH3 \NH2 -CHCH2C(CH3)3 /NOCOCH3 677 I -H -NHC 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 /NOCOCH3 678 I -H -NHC / 1 C Single bond NHSO2CH3 \NH2 I
NHCOOC(CH3)3 \NH2 I
681 -CH ~ -H -NHC// 1 C
OH NHz NHSO2CH3 \NH2 Table 1 (continued) Compound (-D-(CH)m-E-R4) No. -R1 I 5 -R2 -R3 n A Broken line R
-CHCH2C(CH3)3 ~~NOCOCH3 1 C
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 -H ~/NOCOCH3 1 C
NHSO2CH3 NHC\NH
z 685 -CHCH2-C) H -NHC 1 C Single bond NHCOOC(CH33)3 \NH2 686 CHCH2-C H -NHC 1 C Single bond NHSO2CH3 \NH2 -T-----687 -CH~ -H -NHC// 1 C Single bond OH \NH2 688 CHCH2-{'`--~~) -H -NHC 1 C Single bond NHSO2CH3 \NH2 -CHCH2C(CH3)3 NOCH3 689 1 -H -NHC 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 /NOCH3 690 I -H -NHC / 1 C Single bond NHSO2CH3 \NH2 ~---~
691 -CHCH2-{ H ) //
~ ~--~ -H NOCH3 1 C
NHC
NHCOOC(CH3)3 \NH2 z14a598 Table 1 (continued) Compound 1-D-(CH)m-E-R4 -R2 -R3 n A Broken line No. -R R5 692 -CHCH2-H> -H NOCH3 1 C
-NHC
NHSO2CH3 \NH2 OH \NH2 NHSO2CH3 \NH2 I HCH2C(CH3)3 -H NHC 1 C
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NOCH3 NHSO2CH3 \NH2 697 -CHCH2 -H -NHC 1 C Single bond NHCOOC(CH3)3 \NH2 CHCH ) NCOOCH3 698 2 H -H -NHC// 1 C Single bond NHSO2CH3 \NH2 699 CH O -H -NHC// 1 C Single bond 700 -CHCH2 -H NHC// NCOOCH3 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Comvpoound -R1 (D(GH)mER4) -R2 -R3 n A Broken line -CHCH2C(CH3)3 /NCOOCH3 701 I -H -NHC ~ 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NCOOCH3 702 I -H -NHC// 1 C Single bond NHSO2CH3 \NH2 NHCOOC(CH;03 \NH2 704 -CHCH2 - C) -H -NHC// 1 C
NHSO2CH3 \NHz /~ NCOOCH3 705 -CH-{ H ) -H -NHC// 1 C
OH \-/ ~NHZ
706 -CHCH2 ~~~> -H NHC// 1 C
I --CHCH2C(CH3)3 NCOOCH3 NHCOOC2H5 \NH2 708 -CHCH2C(CH3)3 -H NHC// NCOOCH3 1 C
NHSO2CH3 \NHz 709 -CHCH2 H NHC~r 1 C Single bond NHCOOC(CH3)3 \NHZ
I -NHC
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 /NH
648 I -H -NHC ~ 1 C
NHSO2CH3 \NH2 649 -CHCH2--C) -H -NHC 1 C Single bond NHCOOC(CH33)3 \NH2 ----'r---650 -CHCH2--C) -H -NHC// 1 C Single bond NHSO2CH3 ~ NH2 651 -~H ~ -H NHC 1 C Single bond OH ~ NH2 652 -CHCH2-1c) -H -NHC 1 C Single bond I
NHSO2CH3 \NH2 - - -~-653 -CHCH2C(CH3)3 -H NHC// NCH3 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 // NCH3 654 1 -H -NHC 1 C Single bond NHSO2CH3 \NH2 655 -CHCH2-~H -H -NHC 1 C
NHCOOC(CH3)3 \NH2 c Table 1 (continued) Compound 1-D-(CH)m-E-R4 No. -R _R2 -R3 n A Broken line 656 -CHCH2--C NCHg I -NHC
NHSO2CH3 \NH2 OH ~ NH2 NHSO2CH3 \NH2 659 -CHCH2C(CH3)3 -H NHC// NCH3 NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NCH3 ~^--661 2-C' -H -NHC / 1 C Single bond NHCOOC(CH3)3 \NH2 662 CHCH2 H) H,, -NHC/i 1 C Single bond NHSO2CH3 \NHZ
~- -663 CH H -H NHC 1 C Single bond OH \NHz 664 -CHCH2 -H -NHC 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Compoound R1 (-D-(cH)m-E-R4) -R2 -R3 n A Broken line -CHCH2C(CH3)3 NCOCH
665 1 C Single bond -H _NHC % 3 NHCOOC2H5 \NHz -CHCH2C(CH3)3 NCOCH3 666 -H -NHC// 1 C Single bond NHSO2CH3 \NH2 NHCOOC(CH3)3 \NHZ
668 -CHCH2 H) -H -NHC NCOCH3 1 C
NHSO2CH3 ~NH2 669 -CH ~ -H -NHC// NCOCH3 1 C
Qm ~NH2 670 -CHCH2 r\ -H -NHCNCOCH3 1 C
NHSO2CH3 ~NH2 671 -CHCH2C(CH3)3 -H NCOCH3 1 C
672 -CHCH2C(CH3)3 -H NCOCH3 1 C
-NHC
NHSO2CH3 \NH2 673 -CHCH2 -H -NHC// 1 C Single bond NHCOOC(CH3)3 \NHz Table 1 (continued) Compound 1-D-(CH)m-E-R4 -R2 -R3 n A Broken line No. -R R5 ~~ NOCOCH3 674 -CHCH2-( H> -H -NHC// 1 C Single bond NHSO2CH3~ NHZ
675 -CH ~ -H -NHC// 1 C Single bond OH \NH2 CHCH OcoCH3 676 I 2~ -H ,-NHC 1 C Single bond NHSO2CH3 \NH2 -CHCH2C(CH3)3 /NOCOCH3 677 I -H -NHC 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 /NOCOCH3 678 I -H -NHC / 1 C Single bond NHSO2CH3 \NH2 I
NHCOOC(CH3)3 \NH2 I
681 -CH ~ -H -NHC// 1 C
OH NHz NHSO2CH3 \NH2 Table 1 (continued) Compound (-D-(CH)m-E-R4) No. -R1 I 5 -R2 -R3 n A Broken line R
-CHCH2C(CH3)3 ~~NOCOCH3 1 C
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 -H ~/NOCOCH3 1 C
NHSO2CH3 NHC\NH
z 685 -CHCH2-C) H -NHC 1 C Single bond NHCOOC(CH33)3 \NH2 686 CHCH2-C H -NHC 1 C Single bond NHSO2CH3 \NH2 -T-----687 -CH~ -H -NHC// 1 C Single bond OH \NH2 688 CHCH2-{'`--~~) -H -NHC 1 C Single bond NHSO2CH3 \NH2 -CHCH2C(CH3)3 NOCH3 689 1 -H -NHC 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 /NOCH3 690 I -H -NHC / 1 C Single bond NHSO2CH3 \NH2 ~---~
691 -CHCH2-{ H ) //
~ ~--~ -H NOCH3 1 C
NHC
NHCOOC(CH3)3 \NH2 z14a598 Table 1 (continued) Compound 1-D-(CH)m-E-R4 -R2 -R3 n A Broken line No. -R R5 692 -CHCH2-H> -H NOCH3 1 C
-NHC
NHSO2CH3 \NH2 OH \NH2 NHSO2CH3 \NH2 I HCH2C(CH3)3 -H NHC 1 C
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NOCH3 NHSO2CH3 \NH2 697 -CHCH2 -H -NHC 1 C Single bond NHCOOC(CH3)3 \NH2 CHCH ) NCOOCH3 698 2 H -H -NHC// 1 C Single bond NHSO2CH3 \NH2 699 CH O -H -NHC// 1 C Single bond 700 -CHCH2 -H NHC// NCOOCH3 1 C Single bond NHSO2CH3 \NH2 Table 1 (continued) Comvpoound -R1 (D(GH)mER4) -R2 -R3 n A Broken line -CHCH2C(CH3)3 /NCOOCH3 701 I -H -NHC ~ 1 C Single bond NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NCOOCH3 702 I -H -NHC// 1 C Single bond NHSO2CH3 \NH2 NHCOOC(CH;03 \NH2 704 -CHCH2 - C) -H -NHC// 1 C
NHSO2CH3 \NHz /~ NCOOCH3 705 -CH-{ H ) -H -NHC// 1 C
OH \-/ ~NHZ
706 -CHCH2 ~~~> -H NHC// 1 C
I --CHCH2C(CH3)3 NCOOCH3 NHCOOC2H5 \NH2 708 -CHCH2C(CH3)3 -H NHC// NCOOCH3 1 C
NHSO2CH3 \NHz 709 -CHCH2 H NHC~r 1 C Single bond NHCOOC(CH3)3 \NHZ
Table 1 (continued) Compound -R1 (-D-(cH)m-E-R4) -R2 -R3 n A Broken line 710 -CHCH2 H~ -H -NHC// 1 C Single bond NHSO2CH3 \NH2 711 -CH ~ -H -NHC 1 C Single bond OH \NHZ
.- ~
\ NOCOOCH3 712 -CHCH2-H -NHC 1 C Single bond NHSO2CH~3_ \NH2 -CHCH2C(CH3)3 ~NOCOOCH3 713 I -H -NHC 1 C Single bond NHCOOC2H5 ~NH?
-CHCH2C(CH3)3 /NOCOOCH3 714 -H -NHC ~ 1 C Single bond NHSO2CH3 \NH;
NHCOOC(CH3)3 ~NHl --- -'f--716 -CHCH2-O -H -NHC // NOCOOCHs 1 C
\NH2 OH \NH2 NHSO2CH3 \NH2 Table 1 (continued) Compound R1 (-D-(CH)m-E-R4 -R2 -R3 n A Broken line No. - R5 -CHCH2C(CH3)3 // NOCOOCH3 719 i -H NHC 1 C
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NOCOOCH3 720 i -H -NHC~~ 1 C
NHSO2CH3 \NH2 NOH
721 -CHCH2-~) -H -NHC 1 C Single bond NHCOOC(CH;3)3 NH2 NOH
722 -CHCH2 -CH~ -H -NHC 1 C Single bond NHSO2CH3 \NH2 NOH
723 -CH ~ -H NHC 1 C Single bond OH ~NH2 ~ ~
724 -CHCH2-) -H NOH -NHC / 1 C Single bond -CHCH2C(CH3)3 NOH
725 I -H -NHC 1 C Single bond NHCOOC2H5 \NH2 NOH
726 -CHCH2C(CH3)3 -H -NHC// 1 C Single bond NHSO2CH3 \NH
~ - ~
NOH
727 -CHCH2--s -H -NHC 1 C
NHCOOC(CH3)3 NH2 Table 1 (continued) Compound R1 (DH)mER4) -R2 -R3 n A Broken line No. R5 728 -CHCH2--CH) -H NOH 1 C
I -NHC
NOH
NOH
/ \ -H NHC 1 C
NHSO2CH3 \NH2 NOH
731 -CHCH2C(CH3)3 -H -NHC 1 C
732 -CHCH2C(CH j)3 NOH
733 -CHCH2 H -H _NHC NOCOCHZOH 1 C Single bond NHCOOC(CH;3)3 \NH2 734 -CHCH2 H~ -H NHC NOCOCHZOH 1 C Single bond NHSO2CH3 \NH2 ~H NOCOCHzOH
735 - H NHC/ 1 C Single bond OH \NH2 _NHC 1 C Single bond NHSO2CH3 \NHZ
.- ~
\ NOCOOCH3 712 -CHCH2-H -NHC 1 C Single bond NHSO2CH~3_ \NH2 -CHCH2C(CH3)3 ~NOCOOCH3 713 I -H -NHC 1 C Single bond NHCOOC2H5 ~NH?
-CHCH2C(CH3)3 /NOCOOCH3 714 -H -NHC ~ 1 C Single bond NHSO2CH3 \NH;
NHCOOC(CH3)3 ~NHl --- -'f--716 -CHCH2-O -H -NHC // NOCOOCHs 1 C
\NH2 OH \NH2 NHSO2CH3 \NH2 Table 1 (continued) Compound R1 (-D-(CH)m-E-R4 -R2 -R3 n A Broken line No. - R5 -CHCH2C(CH3)3 // NOCOOCH3 719 i -H NHC 1 C
NHCOOC2H5 \NH2 -CHCH2C(CH3)3 NOCOOCH3 720 i -H -NHC~~ 1 C
NHSO2CH3 \NH2 NOH
721 -CHCH2-~) -H -NHC 1 C Single bond NHCOOC(CH;3)3 NH2 NOH
722 -CHCH2 -CH~ -H -NHC 1 C Single bond NHSO2CH3 \NH2 NOH
723 -CH ~ -H NHC 1 C Single bond OH ~NH2 ~ ~
724 -CHCH2-) -H NOH -NHC / 1 C Single bond -CHCH2C(CH3)3 NOH
725 I -H -NHC 1 C Single bond NHCOOC2H5 \NH2 NOH
726 -CHCH2C(CH3)3 -H -NHC// 1 C Single bond NHSO2CH3 \NH
~ - ~
NOH
727 -CHCH2--s -H -NHC 1 C
NHCOOC(CH3)3 NH2 Table 1 (continued) Compound R1 (DH)mER4) -R2 -R3 n A Broken line No. R5 728 -CHCH2--CH) -H NOH 1 C
I -NHC
NOH
NOH
/ \ -H NHC 1 C
NHSO2CH3 \NH2 NOH
731 -CHCH2C(CH3)3 -H -NHC 1 C
732 -CHCH2C(CH j)3 NOH
733 -CHCH2 H -H _NHC NOCOCHZOH 1 C Single bond NHCOOC(CH;3)3 \NH2 734 -CHCH2 H~ -H NHC NOCOCHZOH 1 C Single bond NHSO2CH3 \NH2 ~H NOCOCHzOH
735 - H NHC/ 1 C Single bond OH \NH2 _NHC 1 C Single bond NHSO2CH3 \NHZ
Table 1 (continued) Comvpoound R1 (D(GH)mER4) -R2 -R3 n A Broken line -CHCH2C(CH3)3 NOCOCH2OH
737 I -H NHC 1 C Single bond NHCOOC2H5 \NH2 --_i -CHCH2C(CH3)3 /~NocoCH2oH
738 I -H -NHC 1 C Single bond NHSO2CH3 \NHz 739 -CHCH - HJ H ~NOCOCH2OH 1 C
NHCOOC(CH3)3 \NHZ
740 -CHCH2 H ~ -H -NHC NOCOCH2OH 1 C
NHSO2CH3 ~NH2 -CH -H -H NOCOCHzOH 1 C
741 -NHc OH \NHZ
742 -CHCH2 ~~> -H ~NOCOCH2OH 1 c -NHC
NHSO2CH3 ~NHZ
-CHCH2C(CH3)3 NOCOCH2OH
743 -H -NHC 1 c NHCOOC2H5 \NHz 744 -CHCH2C(CH3)3 -H ~~NOCOCHZOH 1 C
-NHC
NHSO2CH3 \NH2 745 -CH -H -NH2 1 C Single bond Table 1 (continued) Compound 1-D-(CH)m-E-R4 No. -R _R2 -R3 I A Broken line R
746 -CHCH2-CH~ -H -NH2 1 C Single bond I
747 -CHCH2 -CH -H -NH2 1 C Single bond 748 -CHCH2 -~H -H -NH2 1 C Single bond NHCOOCH(CH3)2 749 -CHCH2 -H -NH2 1 C Single bond NHCOOC(CH3)3 750 -CH (~) -H -NH2 1 C Single bond OH
751 -CHCH2 r-\
I -H -NH2 1 C Single bond - ~ --CHCH ~ ~
752 i 2 -H -NH2 1 C Single bond 753 -CHCH2 ~~ -H -NH2 1 C Single bond NHCOOCH(CH3)2 Table 1 (continued) Compound R1 (D(GH)mER4) -R2 -R3 I A Broken line 754 -CHCH2 (`~ -H -NH2 1 C Single bond I
NHCOOC(CH3)3 755 - I , CHCH2 4\
-H -NH2 1 C Single bond 756 -CH -H -NH2 1 C Single bond OH
-CHCH2C(CH3)3 -H -NH2 Tic Single bond -CHCH2C(CH3)3 758 1 -H -NH2 1 C Single bond NHCOOCH(CH3)2 760 -CHCH2-Ho _H -NH2 1 C
I
NHCOOCH(CH3)2 Table 1 (continued) Comvpoound -R1 D-(CH)m-E-R4 -R2 -R3 n A Broken line I -(D -H -NH2 1 C
NHCOOCH(CH3)2 764 "CH -(H -H -NH2 1 C
NHCOOC(CH,3)3 765 -CHCH2--~H -H -NH2 1 C
NHCOOC(CH3)3 766 "CH -(~] -H -NH2 1 C
NHCOOCH(CH3)2 767 -CH -<8 -H -NH2 1 C
NHCOOC(CH3)3 768 -CH -(~) -H -N
770 -(CH2)3 -H -NH2 1 C
771 -CH2OCH2--(' `) -H -NH2 1 C
737 I -H NHC 1 C Single bond NHCOOC2H5 \NH2 --_i -CHCH2C(CH3)3 /~NocoCH2oH
738 I -H -NHC 1 C Single bond NHSO2CH3 \NHz 739 -CHCH - HJ H ~NOCOCH2OH 1 C
NHCOOC(CH3)3 \NHZ
740 -CHCH2 H ~ -H -NHC NOCOCH2OH 1 C
NHSO2CH3 ~NH2 -CH -H -H NOCOCHzOH 1 C
741 -NHc OH \NHZ
742 -CHCH2 ~~> -H ~NOCOCH2OH 1 c -NHC
NHSO2CH3 ~NHZ
-CHCH2C(CH3)3 NOCOCH2OH
743 -H -NHC 1 c NHCOOC2H5 \NHz 744 -CHCH2C(CH3)3 -H ~~NOCOCHZOH 1 C
-NHC
NHSO2CH3 \NH2 745 -CH -H -NH2 1 C Single bond Table 1 (continued) Compound 1-D-(CH)m-E-R4 No. -R _R2 -R3 I A Broken line R
746 -CHCH2-CH~ -H -NH2 1 C Single bond I
747 -CHCH2 -CH -H -NH2 1 C Single bond 748 -CHCH2 -~H -H -NH2 1 C Single bond NHCOOCH(CH3)2 749 -CHCH2 -H -NH2 1 C Single bond NHCOOC(CH3)3 750 -CH (~) -H -NH2 1 C Single bond OH
751 -CHCH2 r-\
I -H -NH2 1 C Single bond - ~ --CHCH ~ ~
752 i 2 -H -NH2 1 C Single bond 753 -CHCH2 ~~ -H -NH2 1 C Single bond NHCOOCH(CH3)2 Table 1 (continued) Compound R1 (D(GH)mER4) -R2 -R3 I A Broken line 754 -CHCH2 (`~ -H -NH2 1 C Single bond I
NHCOOC(CH3)3 755 - I , CHCH2 4\
-H -NH2 1 C Single bond 756 -CH -H -NH2 1 C Single bond OH
-CHCH2C(CH3)3 -H -NH2 Tic Single bond -CHCH2C(CH3)3 758 1 -H -NH2 1 C Single bond NHCOOCH(CH3)2 760 -CHCH2-Ho _H -NH2 1 C
I
NHCOOCH(CH3)2 Table 1 (continued) Comvpoound -R1 D-(CH)m-E-R4 -R2 -R3 n A Broken line I -(D -H -NH2 1 C
NHCOOCH(CH3)2 764 "CH -(H -H -NH2 1 C
NHCOOC(CH,3)3 765 -CHCH2--~H -H -NH2 1 C
NHCOOC(CH3)3 766 "CH -(~] -H -NH2 1 C
NHCOOCH(CH3)2 767 -CH -<8 -H -NH2 1 C
NHCOOC(CH3)3 768 -CH -(~) -H -N
770 -(CH2)3 -H -NH2 1 C
771 -CH2OCH2--(' `) -H -NH2 1 C
Table 1 (continued) Compound -D-(CH)m-E-R4 No. -R1 I 5 -R2 -R3 n A Broken line R
773 -CH(CH2)2 4\ COOCH3 -H -NH
_ 2 1 C
774 -CHCH2O ( \ COOH -H -NH
COOCH2 4\
775 -CHCH2O ~ \ -H -NH2 1 C
I
776 -CHCH2 ~ \> -H -NH2 1 C
I
777 -CH2CH e\
I _ NHCHO
779 -CHCH2 4_\ -H -NH2 1 C
773 -CH(CH2)2 4\ COOCH3 -H -NH
_ 2 1 C
774 -CHCH2O ( \ COOH -H -NH
COOCH2 4\
775 -CHCH2O ~ \ -H -NH2 1 C
I
776 -CHCH2 ~ \> -H -NH2 1 C
I
777 -CH2CH e\
I _ NHCHO
779 -CHCH2 4_\ -H -NH2 1 C
Table 1 (continued) Compound -D-(CH)m-E-R4 No. -R1 I 5 -R2 'R3 n A Broken line R
I
NHCOOCH(CH3)2 - ~- -782 -CHCH2 ~ ~\ -H -NH2 1 C
NHCOOC(CH3)3 OH
784 -CHCH2 4~\ -H -NH2 1 C
OCOCzH5 785 -CHCH2 4~\ -H -NH2 1 C
786 -CHCH2 4\ -H -NH2 1 C
I
I
OCONHCH2CH=CH2 788 -CHCH2C(CH3)3 -H -NH 1 C
I
NHCOOCH(CH3)2 - ~- -782 -CHCH2 ~ ~\ -H -NH2 1 C
NHCOOC(CH3)3 OH
784 -CHCH2 4~\ -H -NH2 1 C
OCOCzH5 785 -CHCH2 4~\ -H -NH2 1 C
786 -CHCH2 4\ -H -NH2 1 C
I
I
OCONHCH2CH=CH2 788 -CHCH2C(CH3)3 -H -NH 1 C
Table 1 (continued) Comvpoound R1 (D(GH)mER4) -R2 -R3 n A Broken line R' -CH(CH2)2SCH3 790 -CH(CH2)3CH3 -H NH2 I Tic 791 -CH(CH2)4CH3 -H -NH2 1 C
-CH(CH2)2COOH
NHS02\--j 793 -CHC(SCH3)(CH3)2 -H
NH2 Ji C
794 -CHCH2C(CH3)3 -H -NH2 1 C
-CHCH2CH(C2H5)2 796 -CH(CH2)4CH3 -H -NH2 1 C
-CHCH2C(CH3)3 797 i -H -NH2 Tic NHCOOCH(CH3)2 798 CHCH2CH(C2H,5)2 _H -NH2 1 C
NHCOOCH(CH3)2 Table 1 (continued) Compoound R1 (-D-(cH)m.ER4) -R2 -R3 n A Broken line HCH2C(CH3)3 -H -NH2 1 C
I
NHCOOC(CH3)3 800 -CHCH2CH(C2H5)2 -H NH2 1 C
NHCOOC(CH3)3 ~
801 -CH(CH2)2SCH3 NHCOOC(CH3)3 -CHCH2C(CH3)3 802 NHCOOCH2 /_ \ -H -NH2 1 c 803 -CHCH2C(CH3)3 -H -NH2 Tic OH
-CHCH2C(CH3)3 -H -NH2 1 C
804 ~
-CHCH2CH(CH3)2 -CHCH(CH3)2 -CHC(CH3)3 808 -CHCH2SC(CH3)3 -H ~ -NH2 1 C
-CH(CH2)2COOH
NHS02\--j 793 -CHC(SCH3)(CH3)2 -H
NH2 Ji C
794 -CHCH2C(CH3)3 -H -NH2 1 C
-CHCH2CH(C2H5)2 796 -CH(CH2)4CH3 -H -NH2 1 C
-CHCH2C(CH3)3 797 i -H -NH2 Tic NHCOOCH(CH3)2 798 CHCH2CH(C2H,5)2 _H -NH2 1 C
NHCOOCH(CH3)2 Table 1 (continued) Compoound R1 (-D-(cH)m.ER4) -R2 -R3 n A Broken line HCH2C(CH3)3 -H -NH2 1 C
I
NHCOOC(CH3)3 800 -CHCH2CH(C2H5)2 -H NH2 1 C
NHCOOC(CH3)3 ~
801 -CH(CH2)2SCH3 NHCOOC(CH3)3 -CHCH2C(CH3)3 802 NHCOOCH2 /_ \ -H -NH2 1 c 803 -CHCH2C(CH3)3 -H -NH2 Tic OH
-CHCH2C(CH3)3 -H -NH2 1 C
804 ~
-CHCH2CH(CH3)2 -CHCH(CH3)2 -CHC(CH3)3 808 -CHCH2SC(CH3)3 -H ~ -NH2 1 C
_214059$
Table 1 (continued) Compoound -R1 (D(cH)mER4) -R2 -R3 n A Broken line R' -CHCH20C(CH3)3 810 -CHCH2OC(CH3)2C2H5 -H -NH2 1 C
NHSOzCH3 811 -CHCH2O(C2H5)2CH3 -H F -NH2 1 C
-----------------------------CHC(CH3)2SCH3 813 -CHC(CH3)2SC2H5 -H -NH2 1 C
814 -CH -G) -H -NH2 2 C Single bond I
-CHCH ~ I
815 ~ 2-H ~ -H -NH2 2 C Single bond 816 -CHCH2--C ) -H -NH2 2 C Single bond I
817 -CHCH2-( -H -NH2 2 C Single bond NHCOOCH(CH3)2 Table 1 (continued) Compound -R1 (D(CH)mER4) _R2 -R3 n A Broken line 818 -CHCH2 -H -NH2 2 C Single bond NHCOOC(CH3)3 819 -CH-0 -H -NH2 2 C Single bond OH
820 -CHCH2 -H -NH2 2 C Single bond 821 -CHCH2- ~~ -H -NH2 2 C Single bond 822 -CHCH2 (_~ -H -NH2 2 C Single bond NHCOOCH(CH3)2 823 -CHCH2 ~\ -H -NH2 2 C Single bond I _ NHCOOC(CH3)3 I 2 2 C Single bond 825 -CH -H -NH2 2 C Single bond I
OH
826 CHCH2C(CH3)3 -H -NH2 2 C Single bond - 2.~4Q598 Table 1 (continued) Co npoound -RI
(D(CH)mER4) -R2 -R3 n A Broken line -CHCH2C(CH3)3 827 1 -H -NH2 2 C Single bond NHCOOCH(CH3)2 828 -CH <D -H -NH2 2 C
829 -C HCH2- o -H -NH2 2 C
830 CHCH2-~ -H -NH2 2 C
831 -CHCH2--o -H -NH2 2 C
NHCOOCH(CH3)2 NHCOOC(CH3)3 833 - CH-~ -H -NH2 ;2 C
I
OH
Table 1 (continued) Compoound -R1 (D(cH)mER4) -R2 -R3 n A Broken line R' -CHCH20C(CH3)3 810 -CHCH2OC(CH3)2C2H5 -H -NH2 1 C
NHSOzCH3 811 -CHCH2O(C2H5)2CH3 -H F -NH2 1 C
-----------------------------CHC(CH3)2SCH3 813 -CHC(CH3)2SC2H5 -H -NH2 1 C
814 -CH -G) -H -NH2 2 C Single bond I
-CHCH ~ I
815 ~ 2-H ~ -H -NH2 2 C Single bond 816 -CHCH2--C ) -H -NH2 2 C Single bond I
817 -CHCH2-( -H -NH2 2 C Single bond NHCOOCH(CH3)2 Table 1 (continued) Compound -R1 (D(CH)mER4) _R2 -R3 n A Broken line 818 -CHCH2 -H -NH2 2 C Single bond NHCOOC(CH3)3 819 -CH-0 -H -NH2 2 C Single bond OH
820 -CHCH2 -H -NH2 2 C Single bond 821 -CHCH2- ~~ -H -NH2 2 C Single bond 822 -CHCH2 (_~ -H -NH2 2 C Single bond NHCOOCH(CH3)2 823 -CHCH2 ~\ -H -NH2 2 C Single bond I _ NHCOOC(CH3)3 I 2 2 C Single bond 825 -CH -H -NH2 2 C Single bond I
OH
826 CHCH2C(CH3)3 -H -NH2 2 C Single bond - 2.~4Q598 Table 1 (continued) Co npoound -RI
(D(CH)mER4) -R2 -R3 n A Broken line -CHCH2C(CH3)3 827 1 -H -NH2 2 C Single bond NHCOOCH(CH3)2 828 -CH <D -H -NH2 2 C
829 -C HCH2- o -H -NH2 2 C
830 CHCH2-~ -H -NH2 2 C
831 -CHCH2--o -H -NH2 2 C
NHCOOCH(CH3)2 NHCOOC(CH3)3 833 - CH-~ -H -NH2 ;2 C
I
OH
Table 1 (continued) Compound R1 (-D-(cH)m-E-.R4) -R2 -R3 I A Broken line 836 -CHCH2 r_~\ -H -NH2 2 C
I
NHCOOCH(CH3)2 837 -CHCH2 4!~\ -H -NH2 2 C
I
NHCOOC(CH3)3 838 -CHCH2-~ ~ -H -NH2 2 CF
~
839 -CH /-\ -H -NH2 2 C
OH
-CHCH2C(CH3)3 841 -CHCH2C(CH3)3 -H -NH2 2 C
NHCOOCH(CH3)2 842 -CH -0 -CH3 -NH2 1 C Single bond 843 -CHCH2-CH -CH3 -NH2 1 C Single bond 844 -CHCH2-CH -CH3 -NH2 1 C Single bond I
I
NHCOOCH(CH3)2 837 -CHCH2 4!~\ -H -NH2 2 C
I
NHCOOC(CH3)3 838 -CHCH2-~ ~ -H -NH2 2 CF
~
839 -CH /-\ -H -NH2 2 C
OH
-CHCH2C(CH3)3 841 -CHCH2C(CH3)3 -H -NH2 2 C
NHCOOCH(CH3)2 842 -CH -0 -CH3 -NH2 1 C Single bond 843 -CHCH2-CH -CH3 -NH2 1 C Single bond 844 -CHCH2-CH -CH3 -NH2 1 C Single bond I
Table 1 (continued) Compound 1-D-(CH)m-E-R4 -R2 -R3 I A Broken line No. -R R5 -{ H) -CH3 -NH2 1 C Single bond I ~
NHCOOCH(CH3)2 846 CHCH2-C -CH3 -NH2 1 C Single bond NHCOOC(CH3)3 847 -CH ~ -CH3 -NH2 1 C Single bond I
OH -;-848 CHCH2 -CH3 -NH2 1 C Single bond 849 -CHCH2-(\) -CH3 -NH2 1 C Single bond 850 -CHCH2 ~~ -CH3 -NH2 1 C Single bond NHCOOCH(CH3)2 851 CHCH ~
2 -CH3 -NH2 1 C Single bond NHCOOC(CH3)3 852 CHCH24C) -CH3 -NH2 1 C! Single bond Table 1 (continued) Comvpoound -R1 (-D-(GH)m-E-R4) -R2 -R3 n A Broken line 853 -CH /\ -CH3 -NH2 1 C Single bond OH
-CHCH2C(CH3)3 854 i -CHg -NH2 1 C Single bond -CHCH2C(CH3)3 855 i -CH3 -NH2 1 C Single bond NHCOOCH(CH3)2 856 -CH~ -CH3 -NH2 1 C
~------857 -CHCHZ-- H ~~ -CH3 -NHz 1 C
NHSOzCH3 858 -CHCH2-( H -CH3 -NH2 1 C
* ~ ~
859 -CHCH2--~H -CH3 -NH2 1 C
I
NHCOOCH(CH3)2 860 -CHCH2-{ -CH3 -NH2 1 C
NHCOOC(CH3)3 -OH
NHCOOCH(CH3)2 846 CHCH2-C -CH3 -NH2 1 C Single bond NHCOOC(CH3)3 847 -CH ~ -CH3 -NH2 1 C Single bond I
OH -;-848 CHCH2 -CH3 -NH2 1 C Single bond 849 -CHCH2-(\) -CH3 -NH2 1 C Single bond 850 -CHCH2 ~~ -CH3 -NH2 1 C Single bond NHCOOCH(CH3)2 851 CHCH ~
2 -CH3 -NH2 1 C Single bond NHCOOC(CH3)3 852 CHCH24C) -CH3 -NH2 1 C! Single bond Table 1 (continued) Comvpoound -R1 (-D-(GH)m-E-R4) -R2 -R3 n A Broken line 853 -CH /\ -CH3 -NH2 1 C Single bond OH
-CHCH2C(CH3)3 854 i -CHg -NH2 1 C Single bond -CHCH2C(CH3)3 855 i -CH3 -NH2 1 C Single bond NHCOOCH(CH3)2 856 -CH~ -CH3 -NH2 1 C
~------857 -CHCHZ-- H ~~ -CH3 -NHz 1 C
NHSOzCH3 858 -CHCH2-( H -CH3 -NH2 1 C
* ~ ~
859 -CHCH2--~H -CH3 -NH2 1 C
I
NHCOOCH(CH3)2 860 -CHCH2-{ -CH3 -NH2 1 C
NHCOOC(CH3)3 -OH
Table 1 (continued) Compound -(D(CH)mER4) R3 n A Broken line No. -R1 1 5 -R2 -R
862 -CHCH2 4\ -CH3 -NH2 1 C
863 -CHCH2 4\ -CH3 -NH2 1 C
864 -CHCH2 -CHg -NH2 1 C
NHCOOCH(CH3)2 865 -CHCH2 n -CH3 -NH2 1 C
NHCOOC(CH3)3 866 -CHCH2 -CH3 -NH2 1 C
867 CH ~_\ -CH3 -NH2 1 C
OH
-CHCH2C(CH3)3 868 1 -CH3 -NH2 1 C
-CHCH2C(CH3)3 NHCOOCH(CH3)2 870 -~H -CH3 -NH2 2 C Single bond Table 1 (continued) Compound 1-D-(CH)m-E-R4 R2 R3 No. -R I A Broken line 871 -CHCH2--< H) -CH3 -NH2 2 C Single bond NHSO2CH~3-872 -CHCH2 -CH> -CH3 -NH2 2 C Single bond 873 -C I HCH2-~H -CH3 -NH2 2 C Single bond NHCOOCH(CH3)2 874 -C I HCH2 -CH3 -NH2 2 C Single bond NHCOOC(CH3)3 875 -CH H -CH3 NH2 2 C Single bond OH
876 -CHCH2 e~\ -CH3 -NH2 2 C Single bond 877 -CHCH2 4_\~ -CH3 -NH2 2 C Single bond 878 -CHCH2 4~\ -CH3 -NH2 2 C Single bond NHCOOCH(CH3)2 Table 1 (continued) Compound -R1 (-D-(CH)m-E-A4) -R2 -R3 n A Broken line 879 -CHCH2 ~~ -CH3 -NH2 2 JC Single bond I
NHCOOC(CH3)3 880 -CHCH2 4\
-CH3 -NH2 2 C Single bond 881 -CH -CH3 -NH2 2 C Single bond OH
-CHCH2C(CH3)3 882 I -CH3 -NH2 2 C Single bond -CHCH2C(CH3)3 883 i -CH3 -NH2 2 C Single bond NHCOOCH(CH3)2 884 -CH -G) -CH3 -NH2 2 C
887 -CHCH2--~H -CH3 -NH2 2 C
I
NHCOOCH(CH3)2 Table 1 (continued) Compound 1-D-(CH)m-E-R4 -R2 -R3 I
No. -R A Broken line 888 -CHCH2--< H ) -CH3 -NH2 2 C
NHCOOC(CH3)3 889 -CH ~ D -CH3 -NH2 2 C
OH
890 -CHCH2 4_~\ -CH3 -NH2 2 C
891 -CHCH2 -~~> -CH3 -NH2 2 C
NHCOOCH(CFi3)2 - ~- , NHCOOC(CH3)3 894 -CHCH24-) 895 -CH ~-~ -CH3 -NH2 2 C
OH
CHCH2C(CH j)3 CHg NH2 2 NHCOOC2H5 I
862 -CHCH2 4\ -CH3 -NH2 1 C
863 -CHCH2 4\ -CH3 -NH2 1 C
864 -CHCH2 -CHg -NH2 1 C
NHCOOCH(CH3)2 865 -CHCH2 n -CH3 -NH2 1 C
NHCOOC(CH3)3 866 -CHCH2 -CH3 -NH2 1 C
867 CH ~_\ -CH3 -NH2 1 C
OH
-CHCH2C(CH3)3 868 1 -CH3 -NH2 1 C
-CHCH2C(CH3)3 NHCOOCH(CH3)2 870 -~H -CH3 -NH2 2 C Single bond Table 1 (continued) Compound 1-D-(CH)m-E-R4 R2 R3 No. -R I A Broken line 871 -CHCH2--< H) -CH3 -NH2 2 C Single bond NHSO2CH~3-872 -CHCH2 -CH> -CH3 -NH2 2 C Single bond 873 -C I HCH2-~H -CH3 -NH2 2 C Single bond NHCOOCH(CH3)2 874 -C I HCH2 -CH3 -NH2 2 C Single bond NHCOOC(CH3)3 875 -CH H -CH3 NH2 2 C Single bond OH
876 -CHCH2 e~\ -CH3 -NH2 2 C Single bond 877 -CHCH2 4_\~ -CH3 -NH2 2 C Single bond 878 -CHCH2 4~\ -CH3 -NH2 2 C Single bond NHCOOCH(CH3)2 Table 1 (continued) Compound -R1 (-D-(CH)m-E-A4) -R2 -R3 n A Broken line 879 -CHCH2 ~~ -CH3 -NH2 2 JC Single bond I
NHCOOC(CH3)3 880 -CHCH2 4\
-CH3 -NH2 2 C Single bond 881 -CH -CH3 -NH2 2 C Single bond OH
-CHCH2C(CH3)3 882 I -CH3 -NH2 2 C Single bond -CHCH2C(CH3)3 883 i -CH3 -NH2 2 C Single bond NHCOOCH(CH3)2 884 -CH -G) -CH3 -NH2 2 C
887 -CHCH2--~H -CH3 -NH2 2 C
I
NHCOOCH(CH3)2 Table 1 (continued) Compound 1-D-(CH)m-E-R4 -R2 -R3 I
No. -R A Broken line 888 -CHCH2--< H ) -CH3 -NH2 2 C
NHCOOC(CH3)3 889 -CH ~ D -CH3 -NH2 2 C
OH
890 -CHCH2 4_~\ -CH3 -NH2 2 C
891 -CHCH2 -~~> -CH3 -NH2 2 C
NHCOOCH(CFi3)2 - ~- , NHCOOC(CH3)3 894 -CHCH24-) 895 -CH ~-~ -CH3 -NH2 2 C
OH
CHCH2C(CH j)3 CHg NH2 2 NHCOOC2H5 I
Table 1 (continued) Co npoound -R1 D-(CH)m-E-R4 -R2 -R3 n A Broken line -CHCH2C(CH3)3 NHCOOCH(CH3)2 898 -CHCH2- H, -H -NHCH3 1 C Single bond NHCOOC(CH3)3 899 -CHCH2-( H~ -H -NHCH3 1 C Single bond I ~
NHSO2CHg 900 -CH -0 -H -NHCH3 1 C Single bond OH
901 -CHCH2-CI) -H -NHCH3 1 C Single bond 902 -CHCH2C(CH3)3 1 -H -NHCH3 1 C Single bond -CHCH2C(CH3)3 903 1 -H -NHCH3 1 C Single bond I
NHCOOC(CH3)3 905 -CHCH2 -C) -H -NHCH3 1 C
NHSO2CHg 900 -CH -0 -H -NHCH3 1 C Single bond OH
901 -CHCH2-CI) -H -NHCH3 1 C Single bond 902 -CHCH2C(CH3)3 1 -H -NHCH3 1 C Single bond -CHCH2C(CH3)3 903 1 -H -NHCH3 1 C Single bond I
NHCOOC(CH3)3 905 -CHCH2 -C) -H -NHCH3 1 C
Table 1 (continued) Compound (D(CH)mER4) No. -R1 I 5 -R2 -R3 n A Broken line R
906 -CH ~ -H -NHCH3 1 c OH
907 -CHCH2 r\ -H -NHCH3 1 C
-CHCH2C(CH3)3 908 -H ~ NHCH3 1 C
-CHCH2C(CH3)3 909 i -H -NHCH3 1 C
910 -CHCH2-< -H -NHC2H5 1 C Single bond I ~---~ .
NHCOOC(CH3)3 911 -CHCH2--C -H -NHC2H5 1 C Single bond 912 -~H -H -NHC2H5 1 C Single bond OH
---f----913 CHCH2--C) -H -NHC2H5 1 C Single bond -CHCH2C(CH3)3 914 ~ -H -NHC2H5 Tic Single bond Table 1 (continued) Compound -R1 -D-(CH)R,-E-R4 _R2 -R3 n A Broken line No. R5 -CHCH2C(CH;;)3 -H -NHC2H5 1 C Single bond 916 -CHCH2-o -H -NHC2H5 1 C
NHCOOC(CH3)3 91 ~ -CHCH2--O -H -NHC2H5 1 C
I
I
OH ~i--919 -CHCH2--C~~ _H -NHC2H5 C
I
-CHCH2C(CH3)3 _H -NHC2H5 T
-C
922 -CHCH2- CH -H -NHCOCH3 1 C Single bond NHCOOC(CH3)3 923 1 C Single bond Table 1 (continued) Compound - -D-(CH)m-E-R4 -R2 -R3 n A Broken line No. R5 924 'CH -H -NHCOCH3 1 C Single bond OH
925 -CHCH2 -H -NHCOCH3 1 C Sin le bond ~ g -CHCH2C(CH3)3 926 1 -H -NHCOCH3 1 C Single bond 927 -CHCH2C(CH;3)3 -H -NHCOCH3 Tic Single bond 928 -CHCH2-o -H -NHCOCH3 1 C
NHCOOC(CH3)3 930 -CH H H`-NHCOCH3 1 C
OH I
- - - ---~--931 -CHCH2 4_` -H -NHCOCH3 1 C
I
-CHCH2C(CH3)3 _214059$
Table 1 (continued) Compound -R1 D-(CH)m-E-R4 -R2 -R3 n A Broken line -CHCH2C(CH3)3 934 -CI HCH2-'G) -H -NHCOOCH3 1 C Single bond NHCOOC(CH3)3 ~-935 -CHCH2--OH -H -NHCOOCH3 1 C Single bond 936 -CH ~ -H -NHCOOCH3 1 C Single bond I
OH
-CHCH2 ~ ~ ~
937 I ~ -H -NHCOOCH3 1 C Single bond 938 -CHCH2C(CH3)3 -H -NHCOOCH3 1 C Single bond I
939 -CHCH2C(CH3)3 -H -NHCOOCH3 1 C Single bond NHSO2CHg 940 -CHCH2--~ -H -NHCOOCH3 1 C
NHCOOC(CH3)3 941 -CHCH2-CH> -H -NHCOOCH3 1 C
906 -CH ~ -H -NHCH3 1 c OH
907 -CHCH2 r\ -H -NHCH3 1 C
-CHCH2C(CH3)3 908 -H ~ NHCH3 1 C
-CHCH2C(CH3)3 909 i -H -NHCH3 1 C
910 -CHCH2-< -H -NHC2H5 1 C Single bond I ~---~ .
NHCOOC(CH3)3 911 -CHCH2--C -H -NHC2H5 1 C Single bond 912 -~H -H -NHC2H5 1 C Single bond OH
---f----913 CHCH2--C) -H -NHC2H5 1 C Single bond -CHCH2C(CH3)3 914 ~ -H -NHC2H5 Tic Single bond Table 1 (continued) Compound -R1 -D-(CH)R,-E-R4 _R2 -R3 n A Broken line No. R5 -CHCH2C(CH;;)3 -H -NHC2H5 1 C Single bond 916 -CHCH2-o -H -NHC2H5 1 C
NHCOOC(CH3)3 91 ~ -CHCH2--O -H -NHC2H5 1 C
I
I
OH ~i--919 -CHCH2--C~~ _H -NHC2H5 C
I
-CHCH2C(CH3)3 _H -NHC2H5 T
-C
922 -CHCH2- CH -H -NHCOCH3 1 C Single bond NHCOOC(CH3)3 923 1 C Single bond Table 1 (continued) Compound - -D-(CH)m-E-R4 -R2 -R3 n A Broken line No. R5 924 'CH -H -NHCOCH3 1 C Single bond OH
925 -CHCH2 -H -NHCOCH3 1 C Sin le bond ~ g -CHCH2C(CH3)3 926 1 -H -NHCOCH3 1 C Single bond 927 -CHCH2C(CH;3)3 -H -NHCOCH3 Tic Single bond 928 -CHCH2-o -H -NHCOCH3 1 C
NHCOOC(CH3)3 930 -CH H H`-NHCOCH3 1 C
OH I
- - - ---~--931 -CHCH2 4_` -H -NHCOCH3 1 C
I
-CHCH2C(CH3)3 _214059$
Table 1 (continued) Compound -R1 D-(CH)m-E-R4 -R2 -R3 n A Broken line -CHCH2C(CH3)3 934 -CI HCH2-'G) -H -NHCOOCH3 1 C Single bond NHCOOC(CH3)3 ~-935 -CHCH2--OH -H -NHCOOCH3 1 C Single bond 936 -CH ~ -H -NHCOOCH3 1 C Single bond I
OH
-CHCH2 ~ ~ ~
937 I ~ -H -NHCOOCH3 1 C Single bond 938 -CHCH2C(CH3)3 -H -NHCOOCH3 1 C Single bond I
939 -CHCH2C(CH3)3 -H -NHCOOCH3 1 C Single bond NHSO2CHg 940 -CHCH2--~ -H -NHCOOCH3 1 C
NHCOOC(CH3)3 941 -CHCH2-CH> -H -NHCOOCH3 1 C
Table 1 (continued) Comvpoound -R1 (-D-(CH)m-E-R4 -R2 -R3 n A Broken line 942 'CH -G) -H -NHCOOCH3 1 C
OH
943 -CHCH2 nl -H -NHCOOCH3 1 C
944 -CHCH2C(CH3)3 -H -NHCOOCH3 1 C
CHCH2C(CH 3)3 H -NHCOOCH3 1 C
945 i 946 -CHCH2-'~ I-1 J -H -NHCOOC(CH3)3 1 C Single bond NHCOOC(~C-H/3)3 947 -CHCH2--(I1 ) -H -NHCOOC(CH3)3 1 C Single bond NHSO2CH3~' 948 -CH ~H) -H -NHCOOC(CH3)3 1 C Single bond OH
949 CHCH2 /_~ H NHCCJOC(CH3)3 1 C Single bond -CHCH2C(CH3)3 950 I -H NHCOOC(CH3)3 1 C Single bond Table 1 (continued) v Compound und R1 (.DH)mER4) -R2 -R3 n A Broken line -CHCH2C(CH3)3 951 i -H -NHCOOC(CH3)3 1 C Single bond 952 CHCH2-~ 1"I ) -H -NHCOOC(CH3)3 1 C
NHCOOC(CH3)3 953 -CHCH2 '( I-1 > -H -NHCOOC(CH3)3 1 C
NHSO2CH~3 /
954 -CH ~ -H -NHCOOC(CH3)3 1 C
OH
955 HCH2 -H -NHCOOC(CH3)3 1 C
-CHCH2C(CH3)3 956 1 -H -NHCOOC(CH3)3 Tic -CHCH2C(CH3)3 957 i -H -NHCOOC(CH3)3 1 C
958 -CHCH2-~ Ii ) -H NHCHZ4'o~o 1 C Single bond NHCOOC(CH3)3 959 -CHCH2 H -H } 0 1 C Single bond NHCH2~ 0 }e 2 c Table 1 (continued) Compound (D(CH)mER4) No. -R1 I -R2 -R3 n A Broken line 960 -OH H -H -NHCHZ-J: }- TC Single bond O o 961 -CHCH2 -H C}H-3o ~ ~ 1 C Single bond NHSO2CH3 -NHCH2 O)~ 0 -CHCH2C(CH3)3 CH3 NHCOOC2H5 -NHCHZ-Co~.o 1 C Single bond -CHCH2C(CH3)3 CH3 963 I -H }-0 1 C Single bond NHSO2CH3 -NHCH2-t0 ~0 964 -CHCH2-{ CH3 NHCOOC(CH3)3 H NHCH2-Co~o 1 C
965 -CHCH2-OH -H C}H-3 1 C
NHSO2CH3 -NHCH2-Lo~o 966 -CH ~ -H -NHCH2-C ~. 1 c OH o 0 967 -CHCH24~ -H ~0 1 C
NHSO2CH3 -NHCHz-{Q~,O
OH
943 -CHCH2 nl -H -NHCOOCH3 1 C
944 -CHCH2C(CH3)3 -H -NHCOOCH3 1 C
CHCH2C(CH 3)3 H -NHCOOCH3 1 C
945 i 946 -CHCH2-'~ I-1 J -H -NHCOOC(CH3)3 1 C Single bond NHCOOC(~C-H/3)3 947 -CHCH2--(I1 ) -H -NHCOOC(CH3)3 1 C Single bond NHSO2CH3~' 948 -CH ~H) -H -NHCOOC(CH3)3 1 C Single bond OH
949 CHCH2 /_~ H NHCCJOC(CH3)3 1 C Single bond -CHCH2C(CH3)3 950 I -H NHCOOC(CH3)3 1 C Single bond Table 1 (continued) v Compound und R1 (.DH)mER4) -R2 -R3 n A Broken line -CHCH2C(CH3)3 951 i -H -NHCOOC(CH3)3 1 C Single bond 952 CHCH2-~ 1"I ) -H -NHCOOC(CH3)3 1 C
NHCOOC(CH3)3 953 -CHCH2 '( I-1 > -H -NHCOOC(CH3)3 1 C
NHSO2CH~3 /
954 -CH ~ -H -NHCOOC(CH3)3 1 C
OH
955 HCH2 -H -NHCOOC(CH3)3 1 C
-CHCH2C(CH3)3 956 1 -H -NHCOOC(CH3)3 Tic -CHCH2C(CH3)3 957 i -H -NHCOOC(CH3)3 1 C
958 -CHCH2-~ Ii ) -H NHCHZ4'o~o 1 C Single bond NHCOOC(CH3)3 959 -CHCH2 H -H } 0 1 C Single bond NHCH2~ 0 }e 2 c Table 1 (continued) Compound (D(CH)mER4) No. -R1 I -R2 -R3 n A Broken line 960 -OH H -H -NHCHZ-J: }- TC Single bond O o 961 -CHCH2 -H C}H-3o ~ ~ 1 C Single bond NHSO2CH3 -NHCH2 O)~ 0 -CHCH2C(CH3)3 CH3 NHCOOC2H5 -NHCHZ-Co~.o 1 C Single bond -CHCH2C(CH3)3 CH3 963 I -H }-0 1 C Single bond NHSO2CH3 -NHCH2-t0 ~0 964 -CHCH2-{ CH3 NHCOOC(CH3)3 H NHCH2-Co~o 1 C
965 -CHCH2-OH -H C}H-3 1 C
NHSO2CH3 -NHCH2-Lo~o 966 -CH ~ -H -NHCH2-C ~. 1 c OH o 0 967 -CHCH24~ -H ~0 1 C
NHSO2CH3 -NHCHz-{Q~,O
Table 1 (continued) Compound D-(CH)m-E-R4 No. -R1 1 -R2 R3 n A Broken line R
-CHCH2C(CH3)3 CH3 968 I -H ~- 5, NHCOOC2H5 -NHCHZ-oo 969 -CHCH2C(CH -H 3)3 C}H3 NHSO2C2H5 -NHCH2~Q11~ O 1 C
-CHCH2C(CH3)3 CH3 968 I -H ~- 5, NHCOOC2H5 -NHCHZ-oo 969 -CHCH2C(CH -H 3)3 C}H3 NHSO2C2H5 -NHCH2~Q11~ O 1 C
21405s8 Table 1 (continued) Comvpoound R~ D-(CH)m-E-R41 -R2 -R3 n A Broken line ~
R ~J
NH
970 -CHCH2O--C}COOH -H C 1 C Single bond NHSO2CH3 \NH2 NH
971 -CHCH2 OCH2COOC2H5 -H _C1 C Single bond NHSO2CH3 \NH2 --- ~
NH
972 CHCH2--c) -H C1 C Single bond NHCOOC2H5 \NH2 -CH(CH2)4CH3 /NH
973 1 -H _C ~ 1 C Single bond NHSO2CH3 \NH2 NH
974 -CHCH2O -H C// 1 C Single bond NHSO2CH3 CH2COOH \NH2 NH
975 -CHCH2O r~_ CH2COOH -H C// 1 C Single bond NHSO2CH3 \NH2 -CH(CH2)4CH3 NH
976 1 -H _C 1 C Single bond NHSO2CH2COOC2H5 \NH2 977 -CHCH2OC(CH3)2C2H5 -H ~NH C 1 C
NHCOOCH(CH3)2 \NH2 CHCH20C(CH3)2C2H5 -H 978 I H _C 1 C
NHCOOC2H5 \NH
979 -CHCH2OC(C2H5)2CHg -H CNH I C
NHCOOCH(CH3)2 \NH2 Table 1 (continued) Comvpoound R1 -D-(CH)m-E-R4 -R2 -R3 n A Broken line -CHCH2SC(CH3)3 / NH
980 1 -H _C / 1 c NHCOOC2H5 \NH2 CH NH
981 -CHCH2O~ -H _C1 C
NHCOOCH(CH3)2 \NH2 -CHCH(CH3)OC(CH3)3 -H /NH 1 C
NHCOOCH(CH3)2 C\NH2 -CHC(CH3)2SCH(CH3)2 //NH C
NHCOOC2H5 \NH2 NOH
984 -CHCH2 -H -C// 1 C Single bond NHCOOCH2COOC2H5 \NH2 NOH
985 -~H~ -H -C 1 C Single bond NHCOOC2H5 \NH2 s NOH
986 '~H I/ -H _G// 1 C Single bond NHCOOC2H5 \NH2 NOH
987 CH{^}F -H _C// 1 C Single bond NHCOOC2H5 \NH2 988 i -H -C 1 C Single bond NHCOOCH2 -(F) NH2 -CHCH2C(CH3)3 /NOH
989 I -H -C / 1 C Single bond NHCOOC(CH3)3 \NH2 '2140598 Table 1 (continued) Compound -R1 (D(CH)mER4 -R2 -R3 n A Broken line 1 C Single bond NHCON(CH3)2 \NH2 -CHCH2COOC(CH3)3 NOH
991 I -H -C // 1 C Single bond \NH2 NHCOOC(CH3)3 \NH2 993 -CHCH(CH3)OC(CH3)3 -H // NOH 1 C
NHCOOCH(CH3)2 C\NH2 NOH
OCOCH3 \NH2 CH NOH
NHCOOCH(CH3)3 i \NH2 996 -CHCH2OC(CH3)3 -H NOCOOCH3 1 C
I -C
NHCOOC2H5 \NH2 997 -CHCH2CH(CH3)2 -H c// NOCOOC2H5 1 C
OH \NH2 - ---CHCH2OC(CH;3)3 -H NOCOCH3 1 C
I -C
NHCOOC2H5 \NH2 999 -CHCH2OC(CH3)3 -H -C // NOCOOCH3 1 C
NHCOOCH(CH3)2 \NH2 Table 1 (continued) Compound -R1 -D-(CH)m-E-R4 -R2 -R3 I A Broken line -CHCH2C(CH3)3 NCOOC2H5 1000 1 -H _C // 1 C Single bond NHSO2CH3 \NHZ
1-0 H -H _~// 1 C Single bond NHSO2CH3 \NHZ
1002 -CHCH2 ~ OCH3 -H -NH2 1 C
-CHCH2OC(CH3)3 1003 1 -H -NH2 Mic 1004 -CH -0 -H -NHCH2/ ~. 1 C
-CHCH2C(CH3)3 -CHCH2C(CH3)3 -H C~(H'3o 1 C
NHCOOCH(CH3)2 "NHCHz-~o-)`o 1006 -CH -H -NHCH2-C 3,. 1 C
R ~J
NH
970 -CHCH2O--C}COOH -H C 1 C Single bond NHSO2CH3 \NH2 NH
971 -CHCH2 OCH2COOC2H5 -H _C1 C Single bond NHSO2CH3 \NH2 --- ~
NH
972 CHCH2--c) -H C1 C Single bond NHCOOC2H5 \NH2 -CH(CH2)4CH3 /NH
973 1 -H _C ~ 1 C Single bond NHSO2CH3 \NH2 NH
974 -CHCH2O -H C// 1 C Single bond NHSO2CH3 CH2COOH \NH2 NH
975 -CHCH2O r~_ CH2COOH -H C// 1 C Single bond NHSO2CH3 \NH2 -CH(CH2)4CH3 NH
976 1 -H _C 1 C Single bond NHSO2CH2COOC2H5 \NH2 977 -CHCH2OC(CH3)2C2H5 -H ~NH C 1 C
NHCOOCH(CH3)2 \NH2 CHCH20C(CH3)2C2H5 -H 978 I H _C 1 C
NHCOOC2H5 \NH
979 -CHCH2OC(C2H5)2CHg -H CNH I C
NHCOOCH(CH3)2 \NH2 Table 1 (continued) Comvpoound R1 -D-(CH)m-E-R4 -R2 -R3 n A Broken line -CHCH2SC(CH3)3 / NH
980 1 -H _C / 1 c NHCOOC2H5 \NH2 CH NH
981 -CHCH2O~ -H _C1 C
NHCOOCH(CH3)2 \NH2 -CHCH(CH3)OC(CH3)3 -H /NH 1 C
NHCOOCH(CH3)2 C\NH2 -CHC(CH3)2SCH(CH3)2 //NH C
NHCOOC2H5 \NH2 NOH
984 -CHCH2 -H -C// 1 C Single bond NHCOOCH2COOC2H5 \NH2 NOH
985 -~H~ -H -C 1 C Single bond NHCOOC2H5 \NH2 s NOH
986 '~H I/ -H _G// 1 C Single bond NHCOOC2H5 \NH2 NOH
987 CH{^}F -H _C// 1 C Single bond NHCOOC2H5 \NH2 988 i -H -C 1 C Single bond NHCOOCH2 -(F) NH2 -CHCH2C(CH3)3 /NOH
989 I -H -C / 1 C Single bond NHCOOC(CH3)3 \NH2 '2140598 Table 1 (continued) Compound -R1 (D(CH)mER4 -R2 -R3 n A Broken line 1 C Single bond NHCON(CH3)2 \NH2 -CHCH2COOC(CH3)3 NOH
991 I -H -C // 1 C Single bond \NH2 NHCOOC(CH3)3 \NH2 993 -CHCH(CH3)OC(CH3)3 -H // NOH 1 C
NHCOOCH(CH3)2 C\NH2 NOH
OCOCH3 \NH2 CH NOH
NHCOOCH(CH3)3 i \NH2 996 -CHCH2OC(CH3)3 -H NOCOOCH3 1 C
I -C
NHCOOC2H5 \NH2 997 -CHCH2CH(CH3)2 -H c// NOCOOC2H5 1 C
OH \NH2 - ---CHCH2OC(CH;3)3 -H NOCOCH3 1 C
I -C
NHCOOC2H5 \NH2 999 -CHCH2OC(CH3)3 -H -C // NOCOOCH3 1 C
NHCOOCH(CH3)2 \NH2 Table 1 (continued) Compound -R1 -D-(CH)m-E-R4 -R2 -R3 I A Broken line -CHCH2C(CH3)3 NCOOC2H5 1000 1 -H _C // 1 C Single bond NHSO2CH3 \NHZ
1-0 H -H _~// 1 C Single bond NHSO2CH3 \NHZ
1002 -CHCH2 ~ OCH3 -H -NH2 1 C
-CHCH2OC(CH3)3 1003 1 -H -NH2 Mic 1004 -CH -0 -H -NHCH2/ ~. 1 C
-CHCH2C(CH3)3 -CHCH2C(CH3)3 -H C~(H'3o 1 C
NHCOOCH(CH3)2 "NHCHz-~o-)`o 1006 -CH -H -NHCH2-C 3,. 1 C
Hereinafter, the production process for the compounds of the present invention will be explained.
The compounds of the present invention can be produced through any combination of reactions suitable for the desired compounds. Typical reaction schemes will be shown below, but they should not be construed to limit the scope of the present invention.
The compounds of the present invention can be produced through any combination of reactions suitable for the desired compounds. Typical reaction schemes will be shown below, but they should not be construed to limit the scope of the present invention.
,~~, (Reaction scheme I) (CH2)n (CH2)n 0 H ~ N
cCOOH + N N R, (II) CN (IV) (III) (CH2) (CH2) 0 R'COOH
N N
H R2 (NA
(VI) (V) CN C=0 CN
(CH92NH N
C=0 R1 (VII) NH2 (CH2) O
C=0 RI ~ (VIII) NH2 (CH2)n (V1) N
C=0 RI1 (IX) NH2 (CH2) 0 R2$?
N R2 NOR2a C=0 R~ (X) NH2 (Reaction scheme II) H2 ~
) (II) + HN (C~
(XI) Q Q
(XII) O
(CH2)n RiCOOH (CH2)n N N
O UN
(XIII) ON
Q C~ Q
(XIV) R
(CH2) N (CH2) O
C_O NH2 C_O NH
(XV) I 1 (XVI) (CH2)n O
(XV) N
(J , R29 R
_0 11 (XVII) H
R
cCOOH + N N R, (II) CN (IV) (III) (CH2) (CH2) 0 R'COOH
N N
H R2 (NA
(VI) (V) CN C=0 CN
(CH92NH N
C=0 R1 (VII) NH2 (CH2) O
C=0 RI ~ (VIII) NH2 (CH2)n (V1) N
C=0 RI1 (IX) NH2 (CH2) 0 R2$?
N R2 NOR2a C=0 R~ (X) NH2 (Reaction scheme II) H2 ~
) (II) + HN (C~
(XI) Q Q
(XII) O
(CH2)n RiCOOH (CH2)n N N
O UN
(XIII) ON
Q C~ Q
(XIV) R
(CH2) N (CH2) O
C_O NH2 C_O NH
(XV) I 1 (XVI) (CH2)n O
(XV) N
(J , R29 R
_0 11 (XVII) H
R
(Reaction scheme III) (CH2)n 0 (II) + HN
~ R2 N NR25 (XVIII) NH2 Q
(XIX) NH2 (CH2) O R1COOH (CH2) O
N -ft ( j--1' N
N + 2 NR25 N 1 25 --/< C=0 (XX) NH2 RI ' (XXI) NH2 wherein R1, R2, R25, n and broken line are as defined above; Q is an amino-protecting group, such as benzyloxycarbonyl group, tertiary butyloxycarbonyl group, etc.; Z is a leaving group such as halogen atom, methanesulfonyloxy group, toluenesulfonyloxy group, trifluoromethylsulfonyloxy group, acetoxy (acetyloxy) group, etc.; R27, R28 and R29 indicate a specific substituent contained in R25 and R26; R27 is a C1-C6 alkyl group, a C2-C7 acyl group or a C2-C7 alkoxycarbonyl group; R28 is a Cl-C6 alkyl group, a C1-C7 acyl group, a C2-C7 alkoxycarbonyl group or a C2-C7 hydroxyalkylcarbonyl group;_R29 is a Cy-C6 alkyl group, a C2-C7 acyl group, a C2-C7 alkoxycarbonyl group or 5-Ci-C3 alkyl-1,3-dioxol-2-on-4-ylmethyl group.
In the above reaction schemes, a known method for synthesizing amide can be used for synthesizing the compounds (IV), (VI), (XII), (XIV), (XIX) and (XXI). There are various methods, for example, a method using ,:~
214059~
dehydrating agents such as dicyclohexylcarbodiimide, 1-ethyl-3-(dimethylaminopropyl)carbodiimide, carbonyldiimidazole, etc., azido method, acid halide method, acid anhydride method, active ester method and the like.(e.q., see, "JIKKEN KAGAKU KOZA, 22, YUKI-GOSEI IV", pp. 259 - (1992), ed. "JAPAN Chemical Society", 4th. edition, published by Maruzen). The reaction is conducted under cooling or heating (or at room temperature) using an inert solvent such as tetrahydrofuran, diethyl ether, dichloromethane, etc.
in a conventional manner. In the above schemes, the compounds (V), (XIII), (XV) and (XX) can be synthesized by deprotection according to a method known in peptide chemistry (e.g. see "The Principle and Experimental Procedures of Peptide Synthesis" written by Nobuo IZUMIYA et al., published by Maruzen).
Further, the compound (VII) is synthesized by reacting imidate, which is obtained by reacting the compound (VI) with alcohol and ari inorganic acid such as hydrochloric acid, with ammonia or an ammonium salt; or by reacting a thioamide compound, which is obtained by reacting the corripound (VI) with hydrogen sulfide in the presence of an organic base such as triethylamine, pyridine, etc., with a lower alkylhalogen compound such as methyl iodide, etc., followed by reacting the resulting thioimidate compound with ammonia or an ammonium salt. Further, the compound (IX) is synthesized by reacting the compound (VI) with hydroxylamine or acid adduct thereof in a suitable solvent such as water, alcohol, tetrahydrofuran, etc. at room temperature or under heating.
Further, the compounds (VIII), (X) and (XVII) are synthesized by reacting the compounds (VII), (IX) and (XV) with R27-Z, R28-Z or R29-.Z in an inert solvent such as tetrahydrofuran, ether, dichloromethane, etc. in the presence of an organic or inorganic base under cooling or heating (or at room temperature), respectively.
Further, the compound (XVI) is synthesized by reacl:ing the compound (XV) with a guanidizing reagent such as 2-alkylisothiourea derivative or acid adduct thereof in a suitable solvent such as water, alcohol, tetrahydrofuran, etc.
at room temperature or under heating.
The respective compounds thus obtained can be isolated and purified by conventional chemical procedures such as extraction, crystallization, recrystallization, various chromatography and the like.
When the compounds of the present invention are used for clinical application, a proportion of a therapeutically active ingredient to a carrier component varies within a range of 1 to 90% by weight. For example, the compounds of the present invention may be orally administered in a dosage form such as granules, fine granules, powders, tablets, hard capsules, soft capsules, syrups, emulsions, suspensions, solutions and the like, or intravenously, intramuscularly or subcutaneously administered in the form of injections. Further, they may also be used in the form of suppositories. They may also be formed into powders which can be converted into solutions or the like for injection before use. There can be used pharmaceutical organic or inorganic solid or liquid carriers or diluents which are suitable for oral, intestinal or parenteral administration to prepare the drugs of the present invention. As the excipient used for preparing solid preparations, for example, there can be used lactose, sucrose, starch, talc, cellulose, dextrin, kaoline, . :ax 2140598 , calcium carbonate and the like. Liquid preparations for oral administration, i.e.
emulsions, syrups, suspensions, solutions, etc. contain inert diluents which are normally used, e.g. water, vegetable oil, etc. This preparation can contain adjuvants such as humectants, suspension auxiliary agents, sweeteners, aromatics, colourants, preservatives, etc., in addition to inert diluents. The resulting liquid preparations may be contained in a capsule of an absorbable substance such as gelatin. As the solvent or suspending agent used for preparing preparations for parenteral administration, i.e. injections, suppositories, etc., for example, there can be used water, propylene glycol, polyethylene glycol, benzyl alcohol, ethyl oleate, lecithin and the like. As the base used for preparing suppositories, for example, there can be used cacao butter, emulsified cacao butter, laurin tallow, witepsol and the like.
Preparations may be prepared by a conventional method.
The clinical dose varies depending upon age, pathology, type of disease and the like. For example, in the case of administering orally to an adult patient, the compounds of the present invention are normally administered with a daily dose of about 0.01 to 1000 mg, preferably 10 to 1000 mg. The pharmaceutical composition of the present invention may be administered 1 to 3 times per day or administered intermittently with the above daily dose.
When used as injections, it is advantageous that the compounds of the present invention are administered continuously or intermittently to an adult patient with a single dose of 0.001 to 100 mg.
The prolineamide derivatives of the present inventioni or the salts thereof have a strong inhibition activity to proteases such as thrombin, trypsin and the like. The compounds of the present invention are also superior in oral absorptive action so that they are useful as oral antithrombin agents, i.,e. oral anticoagulants, or oral antitrypsin agents, i.e. remedy for pancreas diseases such as pancreatitis.
The following Examples and Experimental Examples further illustrate the present invention in detail but are not to be construed to limit the scope thereof.
The conventional abbreviations used in the Examples are as follows:
THF: tetrahydrofuran, DMF: N,N-dimethylformamide, DMSC): dimethyl sulfoxide, CDI: carbonyldiimidazole, DPPA: diphenylphosphorylazide, Z: benzyloxycarbonyl, Boc: tertiary butyloxycarbonyl.
Further, NMR in physical properties stands for nuclear magnetic resonance S is the conventional symbol to indicate chemical shift. TMS
(tetramethylsilane) was used as the internal standard. Further, the numeral shown in parenthesis following the 8 value is the number of hydrogen atoms, and the indications following the number of hydrogen atoms mean that s is singlet, d is doublet, t is triplet, q is quartet, m is multiplet, br is broad absorption peak, respectively.
IR stands for infrared. Spectra were measured as potassium bromide tablets unless otherwise stated. The numerical value means the wave number in cm-' Only the main absorption peaks are reported. Further, mp means the non-corrected melting point in C.
~ R2 N NR25 (XVIII) NH2 Q
(XIX) NH2 (CH2) O R1COOH (CH2) O
N -ft ( j--1' N
N + 2 NR25 N 1 25 --/< C=0 (XX) NH2 RI ' (XXI) NH2 wherein R1, R2, R25, n and broken line are as defined above; Q is an amino-protecting group, such as benzyloxycarbonyl group, tertiary butyloxycarbonyl group, etc.; Z is a leaving group such as halogen atom, methanesulfonyloxy group, toluenesulfonyloxy group, trifluoromethylsulfonyloxy group, acetoxy (acetyloxy) group, etc.; R27, R28 and R29 indicate a specific substituent contained in R25 and R26; R27 is a C1-C6 alkyl group, a C2-C7 acyl group or a C2-C7 alkoxycarbonyl group; R28 is a Cl-C6 alkyl group, a C1-C7 acyl group, a C2-C7 alkoxycarbonyl group or a C2-C7 hydroxyalkylcarbonyl group;_R29 is a Cy-C6 alkyl group, a C2-C7 acyl group, a C2-C7 alkoxycarbonyl group or 5-Ci-C3 alkyl-1,3-dioxol-2-on-4-ylmethyl group.
In the above reaction schemes, a known method for synthesizing amide can be used for synthesizing the compounds (IV), (VI), (XII), (XIV), (XIX) and (XXI). There are various methods, for example, a method using ,:~
214059~
dehydrating agents such as dicyclohexylcarbodiimide, 1-ethyl-3-(dimethylaminopropyl)carbodiimide, carbonyldiimidazole, etc., azido method, acid halide method, acid anhydride method, active ester method and the like.(e.q., see, "JIKKEN KAGAKU KOZA, 22, YUKI-GOSEI IV", pp. 259 - (1992), ed. "JAPAN Chemical Society", 4th. edition, published by Maruzen). The reaction is conducted under cooling or heating (or at room temperature) using an inert solvent such as tetrahydrofuran, diethyl ether, dichloromethane, etc.
in a conventional manner. In the above schemes, the compounds (V), (XIII), (XV) and (XX) can be synthesized by deprotection according to a method known in peptide chemistry (e.g. see "The Principle and Experimental Procedures of Peptide Synthesis" written by Nobuo IZUMIYA et al., published by Maruzen).
Further, the compound (VII) is synthesized by reacting imidate, which is obtained by reacting the compound (VI) with alcohol and ari inorganic acid such as hydrochloric acid, with ammonia or an ammonium salt; or by reacting a thioamide compound, which is obtained by reacting the corripound (VI) with hydrogen sulfide in the presence of an organic base such as triethylamine, pyridine, etc., with a lower alkylhalogen compound such as methyl iodide, etc., followed by reacting the resulting thioimidate compound with ammonia or an ammonium salt. Further, the compound (IX) is synthesized by reacting the compound (VI) with hydroxylamine or acid adduct thereof in a suitable solvent such as water, alcohol, tetrahydrofuran, etc. at room temperature or under heating.
Further, the compounds (VIII), (X) and (XVII) are synthesized by reacting the compounds (VII), (IX) and (XV) with R27-Z, R28-Z or R29-.Z in an inert solvent such as tetrahydrofuran, ether, dichloromethane, etc. in the presence of an organic or inorganic base under cooling or heating (or at room temperature), respectively.
Further, the compound (XVI) is synthesized by reacl:ing the compound (XV) with a guanidizing reagent such as 2-alkylisothiourea derivative or acid adduct thereof in a suitable solvent such as water, alcohol, tetrahydrofuran, etc.
at room temperature or under heating.
The respective compounds thus obtained can be isolated and purified by conventional chemical procedures such as extraction, crystallization, recrystallization, various chromatography and the like.
When the compounds of the present invention are used for clinical application, a proportion of a therapeutically active ingredient to a carrier component varies within a range of 1 to 90% by weight. For example, the compounds of the present invention may be orally administered in a dosage form such as granules, fine granules, powders, tablets, hard capsules, soft capsules, syrups, emulsions, suspensions, solutions and the like, or intravenously, intramuscularly or subcutaneously administered in the form of injections. Further, they may also be used in the form of suppositories. They may also be formed into powders which can be converted into solutions or the like for injection before use. There can be used pharmaceutical organic or inorganic solid or liquid carriers or diluents which are suitable for oral, intestinal or parenteral administration to prepare the drugs of the present invention. As the excipient used for preparing solid preparations, for example, there can be used lactose, sucrose, starch, talc, cellulose, dextrin, kaoline, . :ax 2140598 , calcium carbonate and the like. Liquid preparations for oral administration, i.e.
emulsions, syrups, suspensions, solutions, etc. contain inert diluents which are normally used, e.g. water, vegetable oil, etc. This preparation can contain adjuvants such as humectants, suspension auxiliary agents, sweeteners, aromatics, colourants, preservatives, etc., in addition to inert diluents. The resulting liquid preparations may be contained in a capsule of an absorbable substance such as gelatin. As the solvent or suspending agent used for preparing preparations for parenteral administration, i.e. injections, suppositories, etc., for example, there can be used water, propylene glycol, polyethylene glycol, benzyl alcohol, ethyl oleate, lecithin and the like. As the base used for preparing suppositories, for example, there can be used cacao butter, emulsified cacao butter, laurin tallow, witepsol and the like.
Preparations may be prepared by a conventional method.
The clinical dose varies depending upon age, pathology, type of disease and the like. For example, in the case of administering orally to an adult patient, the compounds of the present invention are normally administered with a daily dose of about 0.01 to 1000 mg, preferably 10 to 1000 mg. The pharmaceutical composition of the present invention may be administered 1 to 3 times per day or administered intermittently with the above daily dose.
When used as injections, it is advantageous that the compounds of the present invention are administered continuously or intermittently to an adult patient with a single dose of 0.001 to 100 mg.
The prolineamide derivatives of the present inventioni or the salts thereof have a strong inhibition activity to proteases such as thrombin, trypsin and the like. The compounds of the present invention are also superior in oral absorptive action so that they are useful as oral antithrombin agents, i.,e. oral anticoagulants, or oral antitrypsin agents, i.e. remedy for pancreas diseases such as pancreatitis.
The following Examples and Experimental Examples further illustrate the present invention in detail but are not to be construed to limit the scope thereof.
The conventional abbreviations used in the Examples are as follows:
THF: tetrahydrofuran, DMF: N,N-dimethylformamide, DMSC): dimethyl sulfoxide, CDI: carbonyldiimidazole, DPPA: diphenylphosphorylazide, Z: benzyloxycarbonyl, Boc: tertiary butyloxycarbonyl.
Further, NMR in physical properties stands for nuclear magnetic resonance S is the conventional symbol to indicate chemical shift. TMS
(tetramethylsilane) was used as the internal standard. Further, the numeral shown in parenthesis following the 8 value is the number of hydrogen atoms, and the indications following the number of hydrogen atoms mean that s is singlet, d is doublet, t is triplet, q is quartet, m is multiplet, br is broad absorption peak, respectively.
IR stands for infrared. Spectra were measured as potassium bromide tablets unless otherwise stated. The numerical value means the wave number in cm-' Only the main absorption peaks are reported. Further, mp means the non-corrected melting point in C.
Example 1 Synthesis of 4-amidino-[(S)-N-((R)-2-methylsulfonylamino-cyclohexylacetyl) prolyl]aminomethylbenzene (compound No. 105 of Table 1) hydrochloride (a) N-4-cyanobenzylphthalimide To a solution of potassium phthalimide (76 g, 410 mrnol) in DMF (250 ml), a solution of 4-cyanobenzyl bromide (73 g, 373 mmol) in THF (250 ml) is added and stirred at 50 C for 3 hours.
Water (500 ml) is added to the mixture and a precipitated crystal was collected. Then, the crystal is washed with water and dried to give 96 g of the title compound (99%). mp: 189-191 C.
(b) 4-Cyano-[(S)-prolyl]aminomethylbenzene hydrochloride To a solution of the corripound (39 g, 150 mmol) obtained in the item (a) in methanol (250 ml), hydrazine hydrate (9 ml) is added and refluxed for 6 hours. After the solvent is evaporated, an aqueous 40% sodium hydroxide solution (300 ml) is added to the residue and stirred.
The reaction mixture is extracted with toluene and the organic layer is washed once with water and saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the resulting crude product (15 g, 73%) is used for the next step.
To a solution of (S)-N-Boc-proline (23.7 g, 110 mmol) in THF (250 ml), CDI (17.8 g, 110 mmol) is added at 0'C.
After the reaction solution is stirred for 2 hours, a solution of the crude ~ :~~:.
product obtained in the above reaction in THF (150 ml) is added. After stirring for 6 hours, the solvent is evaporated and water (300 ml) is added to the residue. The mixture is extracted with chloroform and the organic layer is washed three times with water and once with saturated brine, successively.
After drying over sodium sulfate, the solvent is evaporated and the residue is purified with silica gel chromatography (hexane-ethyl acetate).
The resulting oily product is dissolved in ethyl acetate (100 ml) and a 4N-hydrochloride in ethyl acetate (69 ml) is added and the mixture is stirred at 0 C for 3 hours. The precipitated white solid is collected, washed with ethyl acetate and dried under reduced pressure to give 25.9 g of the titled compound (89%).
NMR (DMSO-d6) 1.80-1.96 (m, 3H), 2.30-2.40 (m, 1H), 3.21 (br, 2H), 4õ26 (br, 1H), 4.44 (d, 2H), 7.49 (d, 2H), 7.82 (d, 2H), 8.59 (br, 1 H), 9.39 (t, 1 H), 10.07 (br, 1 H) (c) 4-Cyano-[(S)-N-((R)-2-t-butyloxycarbonylamino-c:yclohexylacetyl) prolyl]aminomethylbenzene To a solution of the product (21 g, 79 mmol) obtained in the item (b) and (R)-N-t-butyloxycarbonylcyclohexylglycine (20.4 g, 79 mmol) in DMF (200 ml), a solution of triethylamine (22 ml, 159 mmol) and DPPA (22 g, 79 mmol) in DMF (50 ml) is added at 0 C. The mixture is allowed to stand at room temperature and then stirred for 12 hours. Water (400 ml) is added to the reaction mixture which is extracted with toluene-ethyl acetate (1:2). The organic layer is washed three times with water and once with saturated brine, successively, and then dried over sodium sulfate. After the solvent is evaporated, the residue is purified with silica gel chromatography (chloroform-methanol) to give 26.7 g of the titled compound (72%).
NMR (CDCI3) 1.01-1.43 (m, 15H), 1.65-2.38 (m, 9H), 3.57 (q, 1H), 3.96-4.06 (m, 2H), 4.47 (dq, 2H), 4.69 (d, 1 H), 5.12 (d, 1 H), 7.35 (d, 2H), 7.59 (d, 2H), 7.73 (t, 1 H) (d) 4-Cyano-[(S)-N-((R)-2-methylsulfonylamino-cyclohexylacetyl)prolyl]
aminomethylbenzene To a solution of the compound (26.7 g, 57 mmol) obtained in the item (c) in chloroform (50 ml), a 4-N hydrochloride in ethyl acetate (30 ml) is added at 0 C. The mixture is stirred for 3 hours and then the solvent is evaporated.
The resulting residue was dissolved in dichloromethane (250 ml) and triethylamine (19 ml) is added. Then, a solution of methanesulfonyl chloride (7.9 g, 68 mmol) in dichloromethane (50 ml) is added at 0 C and the mixture is stirred for 3 hours. The organic layer is washed once with a saturated sodium bicarbonate solution, water and saturated brine, successively, and then dried over sodium sulfate. The resulting residue is purified with silica gel chromatography (hexane-ethyl acetate) to give 18.6 g of the titled compound (73%).
NMR (CDCI3) 0.9-1.29 (m, 5H), 1.60-1.85 (m, 5H), 2.0-2.4 (m, 5H), 2.89 (s, 3H), 3.55 (q, 1 H), 3.80-3.88 (m, 2H), 4.43 (d, 2H), 4.61 (d, 2H), 5.60 (d, 211), 7.31 (t, 1 H), 7.37 (d, 2H), 7.60 (d, 2H) (e) 4-Amidino-[(S)-N-((R)-2-methylsulfonylamino-cy(,,lohexylacetyl) prolyl]aminomethylbenzene chloride To a solution of the compound (18.6 g, 42 mmol) obtained in the item (d) in chloroform (100 ml), a 37% hydrochloride in ethanol (100 ml) is added at 0 C. The mixture is allowed to stand at 0 C for 48 hours arid then the solvent is evaporated. The resulting residue is dissolved in methanol (100 ml) and ammonium carbonate (16 g, 166 mmol) is added at 0 C. After stirring for 6 hours, the solvent is evaporat6d and the resulting residue is purified with silica gel chromatography (chloroform-methanol) to give 5.2 g of the titled compound (73%).
NMR (DMSO-d6) 9.39 (br, 4H), 8.66 (t, 1 H), 7.81 (d, 2H), 7.48 (d, 2H), 7.40 (m, 1 H), 4.47-4.14 (m, 3H), 3.90 (m, 1 H), 3.71 (m, 1 H), 3.59 (m, 1 H), 2.79 (s, 3H), 2.13 (m, 1 H), 1.88 (m, 3H), 1.69-1.53 (m, 5H), 1.14 (m, 6H) IR: 3366, 2930, 2855, 1636, 1541, 1489, 1451, 1152 According to the same procedures described above, the compounds shown in the following Examples were synthesized.
Example 2 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-4,4-dimethylpentanoyl]
prolyl]aminomethylbenzene (compound No. 104 of Table 1) methanesulfonate NMR (DMSO-d6) 9.31 (br, 2H), 9.11 (br, 2H), 8.60 (t, 1 H), 7.76 (d, 2H), 7.47 (d, 2H), 7.42 (d, 2H), 4.50-4.06 (m, 4H), 3.49 (m, 1 H), 3.71 (m, 1 H), 2.71 (s, 3H), 2.40 (s, 3H), 2.13 (m, 1 H), 1.98 (m, 2H), 1.84 (m, 1 H), 1.48 (d, 2H), 0.98 (s, 9H) IR: 3274, 2957, 1640, 1208, 1150, 1049 214059$
Example 3 4-Amidino-[(S)-N [(R)-2-methylsulfonylamino-3-cyclohexylpropionyl]
prolyl]aminomethylbenzene (compound No. 106 of Table 1) hydrochloride NMR (DMSO-d6) 9.41 (br, 2H), 9.20 (br, 2H), 8.68 (t, 1 H), 7.78 (d, 2H), 7.47 (d, 2H), 7.41 (d, 2H), 4.49-4.23 (m, 3H), 4.13 (m, 1 H), 3.69 (m, 1 H), 3.48 (m, 1 H), 2.72 (s, 3H), 2.12 (m, 1 H), 1.97 (m, 1 H), 1.83 (m, 2H), 1.64 (m, 5H), 1.40 (m, 2H), 1.19 (m, 4H), 0.94 (m, 2H) I R: 3366, 2924, 1640, 1543, 1489, 1449, 1422 Example 4 4-Amidino-[(S)-N [(R)-N'-methylsulfonylphenylalanyl] prolyl]
aminomethylbenzene (compound No. 108 of Table 1) methanesulfonate NMR (DMSO-d6) 9.31 (br, 2H), 9.08 (br, 2H), 8.57 (t, 1 H), 7.75 (d, 2H), 7.71 (d, 1 H), 7.47 (d, 2H), 7.29 (m, 5H), 4.52-4.21 (m, 3H), 3.54 (m, 2H), 3.28 (m, 2H), 3.04 (m, 1 H), 2.90 (m, 2H), 2.71 (s, 3H), 2.50 (s, 3H), 1.88 (m, 2H) IR: 3375, 1663, 1630, 1454, 1327, 1225, 1154, 1046 Example 5 4-Amidino-[(S)-N-[(R)-N'-methylsulfonylmethionyl] prolyi]
aminomethylbenzene (compound No. 110 of Table 1) hydrochloride ..r NMR (DMSO-d6) 2140598 9.45 (br, 2H), 9.26 (br, 2H), 8.68 (t, 1 H), 7.80 (d, 2H), 7.55 (d, 2H), 7.48 (d, 2H), 4.44-4.17 (m, 4H), 3.70 (m, 1 H), 3.59 (m, 1 H), 2.87 (s, 3H), 2.56 (m, 3H), 2.13 (m, 1 H), 2.08 (s, 3H), 1.97 - 1.63 (m, 4H) IR: 3368, 1638, 1543, 1489, 1426, 1314, 1150 Example 6 4-Amidino-[(S)-N-((R)-N'-formylphenylalanyl) prolyl]
aminomethylbenzene (compound No. 94 of Table 1) hydrochloride NMR (DMSO-d6) 9.56 (br, 2H), 9.36 (br, 2H), 8.97 (t, 1 H), 8.70 - 8.60 (m, 1 H), 7.86 (d, 1 H), 7.83 (d, 2H), 7.46 (d, 2H), 7.37-7.17 (m, 5H), 4.36-4.16 (m, 4H), 3.60 - 2.70 (m, 4H), 2.40-1.20 (m, 4H) IR: 3370, 1647, 1541, 1489, 1454, 1404, 704 Example 7 4-Amidino-[(S)-N-((R)-2-methylsulfonylamino-hexanoyl) prolyl]
aminomethylbenzene (compound No. 109 of Table 1) methanesulfonate NMR (DMSO-d6) 9.32 (br, 2H), 9.11 (br, 2H), 8.58 (t, 1 H), 7.76 (d, 2H), 7.48 (d, 2H), 7.42 (d, 1 H), 4.47-4.23 (m, 2H), 4.20-3.90 (m, 3H), 3.54-3.45 (m, 1 H), 3.80-3.66 (m, 1 H), 2.74 (s, 3H), 2.43 (s, 3H), 2.20-0.79 (m, 13H) IR: 3272, 1638, 1543, 1424, 1316, 1206, 1155, 1047 Example 8 4-Amidino-[(S)-N-((R)-2-methylsulfonylamino-4-(4'-niethoxy-carbonyl-phenyl) butanoyl) prolyl]aminomethylbenzene (compound No. 127 of Table 1) hydrochloride NMR (DMSO-d6) 9.35-9.23 (m, 4H), 8.59 (t, 1 H), 7.90 (d, 2H), 7.77 (d, 2H), 7.61 (d, 1 H), 7.47 (d, 2H), 7.40 (d, 2H), 4.44-4.21 (m, 3H), 4.07 (m, 1 H), 3.84 (s, 3H), 3.48 (m, 2H), 2.92-2.63 (m, 3H), 2.77 (s, 3H), 2.12 (m, 1 H), 1.84 (m, 4H) IR: 3370, 1638, 1541, 1489, 1437, 1287, 1150 Example 9 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-3-(3'-carboxyphenoxy) propanoyl] prolyl]aminomethylbenzene (compound No. 130 of Table 1) hydrochloride NMR (DMSO-d6) 9.35 (br, 4H), 8.64 (t, 1 H), 7.78 (d, 2H), 7.71 (d, 1 H), '7.58-7.40 (m, 5H), 7.20 (m, 1 H), 4.62 (m, 1 H), 4.36 (m, 3H), 4.22 (m, 2H), 3.72 (m, 2H), 2.89 (s, 3H), 2.12 (m, 1 H), 1.94 (m, 3H) IR: 3856, 1644, 1543, 1489, 1449, 1316, 1256, 1154 Example 10 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-3-(2'-benzyloxy-carbonylphenoxy) propanoyl] prolyl]aminomethylbenzene (compound No. 123 of Table 1) hydrochloride NMR (DMSO-d6) 9.24 (br, 4H), 8.60 (t, 1 H), 7.77 (d, 2H), 7.71 (m, 1 H), 7.57 (m, 1 H), 7.49-7.35 (m, 8H), 7.16 (d, 1 H), 7.07 (t, 1 H), 5.29 (s, 2H), 4.62 (t, 1 H), 4.37 (m, 3H), 4.28 (m, 1 H), 4.17 (t, 1 H), 3.67 (m, 2H), 2.91 (s, 3H), 2.15 (m, 1 H), 1.88 (m, 3H) IR: 3366, 1642, 1491, 1451, 1314, 1248, 1082 Example 11 4-Amidino-[(S)-N-[(R)-2-ethoxycarbonylamino-3-methyl-3-methylthiobutanoyl] prolyl]aminomethylbenzene (compounci No. 98 of Table 1) hydrochloride NMR (DMSO-d6) 8.89 (br, 2H), 8.66 (br, 2H), 7.77 (d, 2H), 7.33 (d, 2H), 6.27 (d, 1 H), 4.65 (m, 1 H), 4.46 (d, 1 H), 4.37 (m, 2H), 3.97-3.72 (m, 4H), 2.62 (m, 1 H), 2.15 (br, 3H), 2.04 (s, 3H), 1.40 (s, 3H), 1.36 (s, 3H), 1.05 (t, 3H) IR: 3323, 2926, 1635, 1535, 1439, 1242, 1055 Example 12 4-Amidino-[(S)-N-[(R)-2-carboxymethylsulfonylaminoheptanoyl] prolyl]
aminomethylbenzene (compound No. 152 of Table 1) hydrochloride NMR (DMSO-d6) 9.80 (br , 2H), 9.23 (br, 2H), 8.80 (t, 1 H), 7.69 (d, 2H), 7.42 (d, 2H), 7.23 (d, 1 H), 4.51 -4.17 (m, 5H), 3.70 (m, H), 2.11 (m, 1 H), 1.92 (ni, 3H), 1.57-1.28 (m, 8H), 0.87 (m, 3H) IR: 3366, 2957, 1636, 1543, 1489, 1416, 1318, 1136 .2144598 Example 13 4-Amidino-[(S)-N-(4-phenylbutanoyl)prolyl) aminomethylbenzene (compound No. 3 of Table 1) hydrochloride NMR (DMSO-d6) 9.39 (br, 2H), 9.22 (br, 2H), 8.55 (t, 1 H), 7.80 (d, 2H), 7.48 (d, 2H), 7.31-7.13 (m, 5H), 4.37-4.30 (m, 3H), 3.60-3.30 (m, 2H), 2.60 (t, 2H), 2.34-1.75 (m, 8H) IR: 3264, 1618, 1541, 1491, 1451, 702 Example 14 4-Amidino-[(S)-N-(2-benzyloxyacetyl)prolyl) aminomethylbenzene (compound No. 55 of Table 1) hydrochloride NMR (DMSO-d6) 9.41 (br, 2H), 9.23 (br, 2H), 8.66 (t, 1 H), 7.80 (d, 2H), 7.49 (d, 2H), 7.42-7.27 (m, 5H), 4.61-4.08 (m, 7H), 3.56-3.40 (m, 2H), 2.20-1.78 (m, 4H) IR: 3262, 1645, 1539, 1489, 1454, 740 Example 15 Trans-4-amidino-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl}prolyl} aminomethylcyclohexane (compound No. 263 of Table 1) hydrochloride (a) Trans-4-N-benzyloxycarbonylaminomethyl-cyclohexylnitrile To a solution of trans-4-aminomethylcyclohexanecarboxylic acid (25 g, 159 mmol) and sodium carbonate (20 g, 191 mmol) in water (300 ml), benzyloxycarbonyl chloride (27 ml, 190 mmol) is added at 0 C. After stirring for 6 hours, 1 N-hydrochloric acid is added until the pH of the reaction mixture indicates 2, and the precipitated white solid is collected, washed with water and dried. The resulting white solid is dissolved in THF (3C)0 ml) and CDI (21 g, 130 mmol) is added at 0 C. After stirring for 3 hours, the reaction mixture is added dropwise to a mixed solution of 33% ammonia in water (50 ml) and THF
(150 ml) at 0'C. After stirring for 5 hours, the solvent is evaporated and water (500 ml) is added, and the precipitated white solid is collected, washed with water and dried.
To a solution of the resulting compound in 1,2-dichloroethane (500 ml), thionyl chloride (19 ml, 260 mmol) is added and heated to an inner temperature of 70 C. After stirring for 5 hours, the reaction rnixture is poured into ice water and neutralized with an aqueous 1 N-sodium hydroxide solution.
After extracting with chloroform, the organic layer is washed twice with water and once with saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the resulting crude product is recrystallized (hexane-ethyl acetate) to give 22.8 g of the titled compound (53%). mp:90-92 C
(b) Trans-4-(S)-prolylaminomethyl-cyclohexylnitrile The compound obtained in the item (a) is dissolved iri ethanol (250 ml) and the catalytic hydrogenation is conducted at room temperature and atomospheric pressure in the presence of palladium black (1 g). After the completion of the reaction, the catalyst is filtered off and the solvent is evaporated.
Water (500 ml) is added to the mixture and a precipitated crystal was collected. Then, the crystal is washed with water and dried to give 96 g of the title compound (99%). mp: 189-191 C.
(b) 4-Cyano-[(S)-prolyl]aminomethylbenzene hydrochloride To a solution of the corripound (39 g, 150 mmol) obtained in the item (a) in methanol (250 ml), hydrazine hydrate (9 ml) is added and refluxed for 6 hours. After the solvent is evaporated, an aqueous 40% sodium hydroxide solution (300 ml) is added to the residue and stirred.
The reaction mixture is extracted with toluene and the organic layer is washed once with water and saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the resulting crude product (15 g, 73%) is used for the next step.
To a solution of (S)-N-Boc-proline (23.7 g, 110 mmol) in THF (250 ml), CDI (17.8 g, 110 mmol) is added at 0'C.
After the reaction solution is stirred for 2 hours, a solution of the crude ~ :~~:.
product obtained in the above reaction in THF (150 ml) is added. After stirring for 6 hours, the solvent is evaporated and water (300 ml) is added to the residue. The mixture is extracted with chloroform and the organic layer is washed three times with water and once with saturated brine, successively.
After drying over sodium sulfate, the solvent is evaporated and the residue is purified with silica gel chromatography (hexane-ethyl acetate).
The resulting oily product is dissolved in ethyl acetate (100 ml) and a 4N-hydrochloride in ethyl acetate (69 ml) is added and the mixture is stirred at 0 C for 3 hours. The precipitated white solid is collected, washed with ethyl acetate and dried under reduced pressure to give 25.9 g of the titled compound (89%).
NMR (DMSO-d6) 1.80-1.96 (m, 3H), 2.30-2.40 (m, 1H), 3.21 (br, 2H), 4õ26 (br, 1H), 4.44 (d, 2H), 7.49 (d, 2H), 7.82 (d, 2H), 8.59 (br, 1 H), 9.39 (t, 1 H), 10.07 (br, 1 H) (c) 4-Cyano-[(S)-N-((R)-2-t-butyloxycarbonylamino-c:yclohexylacetyl) prolyl]aminomethylbenzene To a solution of the product (21 g, 79 mmol) obtained in the item (b) and (R)-N-t-butyloxycarbonylcyclohexylglycine (20.4 g, 79 mmol) in DMF (200 ml), a solution of triethylamine (22 ml, 159 mmol) and DPPA (22 g, 79 mmol) in DMF (50 ml) is added at 0 C. The mixture is allowed to stand at room temperature and then stirred for 12 hours. Water (400 ml) is added to the reaction mixture which is extracted with toluene-ethyl acetate (1:2). The organic layer is washed three times with water and once with saturated brine, successively, and then dried over sodium sulfate. After the solvent is evaporated, the residue is purified with silica gel chromatography (chloroform-methanol) to give 26.7 g of the titled compound (72%).
NMR (CDCI3) 1.01-1.43 (m, 15H), 1.65-2.38 (m, 9H), 3.57 (q, 1H), 3.96-4.06 (m, 2H), 4.47 (dq, 2H), 4.69 (d, 1 H), 5.12 (d, 1 H), 7.35 (d, 2H), 7.59 (d, 2H), 7.73 (t, 1 H) (d) 4-Cyano-[(S)-N-((R)-2-methylsulfonylamino-cyclohexylacetyl)prolyl]
aminomethylbenzene To a solution of the compound (26.7 g, 57 mmol) obtained in the item (c) in chloroform (50 ml), a 4-N hydrochloride in ethyl acetate (30 ml) is added at 0 C. The mixture is stirred for 3 hours and then the solvent is evaporated.
The resulting residue was dissolved in dichloromethane (250 ml) and triethylamine (19 ml) is added. Then, a solution of methanesulfonyl chloride (7.9 g, 68 mmol) in dichloromethane (50 ml) is added at 0 C and the mixture is stirred for 3 hours. The organic layer is washed once with a saturated sodium bicarbonate solution, water and saturated brine, successively, and then dried over sodium sulfate. The resulting residue is purified with silica gel chromatography (hexane-ethyl acetate) to give 18.6 g of the titled compound (73%).
NMR (CDCI3) 0.9-1.29 (m, 5H), 1.60-1.85 (m, 5H), 2.0-2.4 (m, 5H), 2.89 (s, 3H), 3.55 (q, 1 H), 3.80-3.88 (m, 2H), 4.43 (d, 2H), 4.61 (d, 2H), 5.60 (d, 211), 7.31 (t, 1 H), 7.37 (d, 2H), 7.60 (d, 2H) (e) 4-Amidino-[(S)-N-((R)-2-methylsulfonylamino-cy(,,lohexylacetyl) prolyl]aminomethylbenzene chloride To a solution of the compound (18.6 g, 42 mmol) obtained in the item (d) in chloroform (100 ml), a 37% hydrochloride in ethanol (100 ml) is added at 0 C. The mixture is allowed to stand at 0 C for 48 hours arid then the solvent is evaporated. The resulting residue is dissolved in methanol (100 ml) and ammonium carbonate (16 g, 166 mmol) is added at 0 C. After stirring for 6 hours, the solvent is evaporat6d and the resulting residue is purified with silica gel chromatography (chloroform-methanol) to give 5.2 g of the titled compound (73%).
NMR (DMSO-d6) 9.39 (br, 4H), 8.66 (t, 1 H), 7.81 (d, 2H), 7.48 (d, 2H), 7.40 (m, 1 H), 4.47-4.14 (m, 3H), 3.90 (m, 1 H), 3.71 (m, 1 H), 3.59 (m, 1 H), 2.79 (s, 3H), 2.13 (m, 1 H), 1.88 (m, 3H), 1.69-1.53 (m, 5H), 1.14 (m, 6H) IR: 3366, 2930, 2855, 1636, 1541, 1489, 1451, 1152 According to the same procedures described above, the compounds shown in the following Examples were synthesized.
Example 2 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-4,4-dimethylpentanoyl]
prolyl]aminomethylbenzene (compound No. 104 of Table 1) methanesulfonate NMR (DMSO-d6) 9.31 (br, 2H), 9.11 (br, 2H), 8.60 (t, 1 H), 7.76 (d, 2H), 7.47 (d, 2H), 7.42 (d, 2H), 4.50-4.06 (m, 4H), 3.49 (m, 1 H), 3.71 (m, 1 H), 2.71 (s, 3H), 2.40 (s, 3H), 2.13 (m, 1 H), 1.98 (m, 2H), 1.84 (m, 1 H), 1.48 (d, 2H), 0.98 (s, 9H) IR: 3274, 2957, 1640, 1208, 1150, 1049 214059$
Example 3 4-Amidino-[(S)-N [(R)-2-methylsulfonylamino-3-cyclohexylpropionyl]
prolyl]aminomethylbenzene (compound No. 106 of Table 1) hydrochloride NMR (DMSO-d6) 9.41 (br, 2H), 9.20 (br, 2H), 8.68 (t, 1 H), 7.78 (d, 2H), 7.47 (d, 2H), 7.41 (d, 2H), 4.49-4.23 (m, 3H), 4.13 (m, 1 H), 3.69 (m, 1 H), 3.48 (m, 1 H), 2.72 (s, 3H), 2.12 (m, 1 H), 1.97 (m, 1 H), 1.83 (m, 2H), 1.64 (m, 5H), 1.40 (m, 2H), 1.19 (m, 4H), 0.94 (m, 2H) I R: 3366, 2924, 1640, 1543, 1489, 1449, 1422 Example 4 4-Amidino-[(S)-N [(R)-N'-methylsulfonylphenylalanyl] prolyl]
aminomethylbenzene (compound No. 108 of Table 1) methanesulfonate NMR (DMSO-d6) 9.31 (br, 2H), 9.08 (br, 2H), 8.57 (t, 1 H), 7.75 (d, 2H), 7.71 (d, 1 H), 7.47 (d, 2H), 7.29 (m, 5H), 4.52-4.21 (m, 3H), 3.54 (m, 2H), 3.28 (m, 2H), 3.04 (m, 1 H), 2.90 (m, 2H), 2.71 (s, 3H), 2.50 (s, 3H), 1.88 (m, 2H) IR: 3375, 1663, 1630, 1454, 1327, 1225, 1154, 1046 Example 5 4-Amidino-[(S)-N-[(R)-N'-methylsulfonylmethionyl] prolyi]
aminomethylbenzene (compound No. 110 of Table 1) hydrochloride ..r NMR (DMSO-d6) 2140598 9.45 (br, 2H), 9.26 (br, 2H), 8.68 (t, 1 H), 7.80 (d, 2H), 7.55 (d, 2H), 7.48 (d, 2H), 4.44-4.17 (m, 4H), 3.70 (m, 1 H), 3.59 (m, 1 H), 2.87 (s, 3H), 2.56 (m, 3H), 2.13 (m, 1 H), 2.08 (s, 3H), 1.97 - 1.63 (m, 4H) IR: 3368, 1638, 1543, 1489, 1426, 1314, 1150 Example 6 4-Amidino-[(S)-N-((R)-N'-formylphenylalanyl) prolyl]
aminomethylbenzene (compound No. 94 of Table 1) hydrochloride NMR (DMSO-d6) 9.56 (br, 2H), 9.36 (br, 2H), 8.97 (t, 1 H), 8.70 - 8.60 (m, 1 H), 7.86 (d, 1 H), 7.83 (d, 2H), 7.46 (d, 2H), 7.37-7.17 (m, 5H), 4.36-4.16 (m, 4H), 3.60 - 2.70 (m, 4H), 2.40-1.20 (m, 4H) IR: 3370, 1647, 1541, 1489, 1454, 1404, 704 Example 7 4-Amidino-[(S)-N-((R)-2-methylsulfonylamino-hexanoyl) prolyl]
aminomethylbenzene (compound No. 109 of Table 1) methanesulfonate NMR (DMSO-d6) 9.32 (br, 2H), 9.11 (br, 2H), 8.58 (t, 1 H), 7.76 (d, 2H), 7.48 (d, 2H), 7.42 (d, 1 H), 4.47-4.23 (m, 2H), 4.20-3.90 (m, 3H), 3.54-3.45 (m, 1 H), 3.80-3.66 (m, 1 H), 2.74 (s, 3H), 2.43 (s, 3H), 2.20-0.79 (m, 13H) IR: 3272, 1638, 1543, 1424, 1316, 1206, 1155, 1047 Example 8 4-Amidino-[(S)-N-((R)-2-methylsulfonylamino-4-(4'-niethoxy-carbonyl-phenyl) butanoyl) prolyl]aminomethylbenzene (compound No. 127 of Table 1) hydrochloride NMR (DMSO-d6) 9.35-9.23 (m, 4H), 8.59 (t, 1 H), 7.90 (d, 2H), 7.77 (d, 2H), 7.61 (d, 1 H), 7.47 (d, 2H), 7.40 (d, 2H), 4.44-4.21 (m, 3H), 4.07 (m, 1 H), 3.84 (s, 3H), 3.48 (m, 2H), 2.92-2.63 (m, 3H), 2.77 (s, 3H), 2.12 (m, 1 H), 1.84 (m, 4H) IR: 3370, 1638, 1541, 1489, 1437, 1287, 1150 Example 9 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-3-(3'-carboxyphenoxy) propanoyl] prolyl]aminomethylbenzene (compound No. 130 of Table 1) hydrochloride NMR (DMSO-d6) 9.35 (br, 4H), 8.64 (t, 1 H), 7.78 (d, 2H), 7.71 (d, 1 H), '7.58-7.40 (m, 5H), 7.20 (m, 1 H), 4.62 (m, 1 H), 4.36 (m, 3H), 4.22 (m, 2H), 3.72 (m, 2H), 2.89 (s, 3H), 2.12 (m, 1 H), 1.94 (m, 3H) IR: 3856, 1644, 1543, 1489, 1449, 1316, 1256, 1154 Example 10 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-3-(2'-benzyloxy-carbonylphenoxy) propanoyl] prolyl]aminomethylbenzene (compound No. 123 of Table 1) hydrochloride NMR (DMSO-d6) 9.24 (br, 4H), 8.60 (t, 1 H), 7.77 (d, 2H), 7.71 (m, 1 H), 7.57 (m, 1 H), 7.49-7.35 (m, 8H), 7.16 (d, 1 H), 7.07 (t, 1 H), 5.29 (s, 2H), 4.62 (t, 1 H), 4.37 (m, 3H), 4.28 (m, 1 H), 4.17 (t, 1 H), 3.67 (m, 2H), 2.91 (s, 3H), 2.15 (m, 1 H), 1.88 (m, 3H) IR: 3366, 1642, 1491, 1451, 1314, 1248, 1082 Example 11 4-Amidino-[(S)-N-[(R)-2-ethoxycarbonylamino-3-methyl-3-methylthiobutanoyl] prolyl]aminomethylbenzene (compounci No. 98 of Table 1) hydrochloride NMR (DMSO-d6) 8.89 (br, 2H), 8.66 (br, 2H), 7.77 (d, 2H), 7.33 (d, 2H), 6.27 (d, 1 H), 4.65 (m, 1 H), 4.46 (d, 1 H), 4.37 (m, 2H), 3.97-3.72 (m, 4H), 2.62 (m, 1 H), 2.15 (br, 3H), 2.04 (s, 3H), 1.40 (s, 3H), 1.36 (s, 3H), 1.05 (t, 3H) IR: 3323, 2926, 1635, 1535, 1439, 1242, 1055 Example 12 4-Amidino-[(S)-N-[(R)-2-carboxymethylsulfonylaminoheptanoyl] prolyl]
aminomethylbenzene (compound No. 152 of Table 1) hydrochloride NMR (DMSO-d6) 9.80 (br , 2H), 9.23 (br, 2H), 8.80 (t, 1 H), 7.69 (d, 2H), 7.42 (d, 2H), 7.23 (d, 1 H), 4.51 -4.17 (m, 5H), 3.70 (m, H), 2.11 (m, 1 H), 1.92 (ni, 3H), 1.57-1.28 (m, 8H), 0.87 (m, 3H) IR: 3366, 2957, 1636, 1543, 1489, 1416, 1318, 1136 .2144598 Example 13 4-Amidino-[(S)-N-(4-phenylbutanoyl)prolyl) aminomethylbenzene (compound No. 3 of Table 1) hydrochloride NMR (DMSO-d6) 9.39 (br, 2H), 9.22 (br, 2H), 8.55 (t, 1 H), 7.80 (d, 2H), 7.48 (d, 2H), 7.31-7.13 (m, 5H), 4.37-4.30 (m, 3H), 3.60-3.30 (m, 2H), 2.60 (t, 2H), 2.34-1.75 (m, 8H) IR: 3264, 1618, 1541, 1491, 1451, 702 Example 14 4-Amidino-[(S)-N-(2-benzyloxyacetyl)prolyl) aminomethylbenzene (compound No. 55 of Table 1) hydrochloride NMR (DMSO-d6) 9.41 (br, 2H), 9.23 (br, 2H), 8.66 (t, 1 H), 7.80 (d, 2H), 7.49 (d, 2H), 7.42-7.27 (m, 5H), 4.61-4.08 (m, 7H), 3.56-3.40 (m, 2H), 2.20-1.78 (m, 4H) IR: 3262, 1645, 1539, 1489, 1454, 740 Example 15 Trans-4-amidino-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl}prolyl} aminomethylcyclohexane (compound No. 263 of Table 1) hydrochloride (a) Trans-4-N-benzyloxycarbonylaminomethyl-cyclohexylnitrile To a solution of trans-4-aminomethylcyclohexanecarboxylic acid (25 g, 159 mmol) and sodium carbonate (20 g, 191 mmol) in water (300 ml), benzyloxycarbonyl chloride (27 ml, 190 mmol) is added at 0 C. After stirring for 6 hours, 1 N-hydrochloric acid is added until the pH of the reaction mixture indicates 2, and the precipitated white solid is collected, washed with water and dried. The resulting white solid is dissolved in THF (3C)0 ml) and CDI (21 g, 130 mmol) is added at 0 C. After stirring for 3 hours, the reaction mixture is added dropwise to a mixed solution of 33% ammonia in water (50 ml) and THF
(150 ml) at 0'C. After stirring for 5 hours, the solvent is evaporated and water (500 ml) is added, and the precipitated white solid is collected, washed with water and dried.
To a solution of the resulting compound in 1,2-dichloroethane (500 ml), thionyl chloride (19 ml, 260 mmol) is added and heated to an inner temperature of 70 C. After stirring for 5 hours, the reaction rnixture is poured into ice water and neutralized with an aqueous 1 N-sodium hydroxide solution.
After extracting with chloroform, the organic layer is washed twice with water and once with saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the resulting crude product is recrystallized (hexane-ethyl acetate) to give 22.8 g of the titled compound (53%). mp:90-92 C
(b) Trans-4-(S)-prolylaminomethyl-cyclohexylnitrile The compound obtained in the item (a) is dissolved iri ethanol (250 ml) and the catalytic hydrogenation is conducted at room temperature and atomospheric pressure in the presence of palladium black (1 g). After the completion of the reaction, the catalyst is filtered off and the solvent is evaporated.
To a solution of (S)-N-benzyloxycarbonylproline (20.7 g, 83 mmol) in THF (150 ml), CDI (13.5 g, 83 mmol) is added at 0 C. After stirring for 3 hours, a solution of the compound obtained in the above reaction in THF
(200 ml) is added at 0 C. After stirring for 12 hours, the solvent is evaporated, and chloroform (400 ml) is added to the resulting residue. The organic layer is washed three times with water and once with saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the resulting residue is purified with silica gel chromatography (chloroform-methanol).
The resulting compound is dissolved in ethanol (250 ml) and the catalytic hydrogenation is conducted at room temperature and atomospheric pressure in the presence of palladium black (1 g). After the completion of the reaction, the catalyst is filtered off and the solvent is evaporated to give 18.8 g of the titled compound (95%).
NMR (DMSO-d6) 0.88-1.06 (m, 2H), 1.38-1.52 (m, 3H), 1.68-2.03 (m, 7H), 2.20-2.40 (m, 1 H), 2.52-2.67 (m, 1 H), 2.80-3.20 (m, 4H), 4.03-4.10 (m, 1 H), 7.53 (br, 1 H), 8.65-8.70 (m, 1 H) (c) Trans-4-amidino-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl] prolyl]aminomethylcyclohexane hydrochloride According to the same manner as that described in the items (c) to (e) of Example 1, the titled compound can be synthesized from the compound obtained in the item (b) and (R)-2-t-butyloxycarbonylamino-4,4-dimethylpentanoic acid.
(200 ml) is added at 0 C. After stirring for 12 hours, the solvent is evaporated, and chloroform (400 ml) is added to the resulting residue. The organic layer is washed three times with water and once with saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the resulting residue is purified with silica gel chromatography (chloroform-methanol).
The resulting compound is dissolved in ethanol (250 ml) and the catalytic hydrogenation is conducted at room temperature and atomospheric pressure in the presence of palladium black (1 g). After the completion of the reaction, the catalyst is filtered off and the solvent is evaporated to give 18.8 g of the titled compound (95%).
NMR (DMSO-d6) 0.88-1.06 (m, 2H), 1.38-1.52 (m, 3H), 1.68-2.03 (m, 7H), 2.20-2.40 (m, 1 H), 2.52-2.67 (m, 1 H), 2.80-3.20 (m, 4H), 4.03-4.10 (m, 1 H), 7.53 (br, 1 H), 8.65-8.70 (m, 1 H) (c) Trans-4-amidino-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl] prolyl]aminomethylcyclohexane hydrochloride According to the same manner as that described in the items (c) to (e) of Example 1, the titled compound can be synthesized from the compound obtained in the item (b) and (R)-2-t-butyloxycarbonylamino-4,4-dimethylpentanoic acid.
NMR (DMSO-d6) 8.95 (br, 2H), 8.69 (br, 2H), 7.60 (br, 1 H), 6.32 (br, 1 H), 4.56 (m, 1 H), 4.39 (m, 1 H), 4.18 (q, 2H), 4.10 (m, 1 H), 3.52 (m, 1 H), 3.19 (m, 1 H), 2.89 (m, 1 H), 2.69 (m, 1 H), 2.14-1.59 (m, 12H), 1.26 (t, 3H), 0.98 (s, 9H), 0.98-0.89 (m, 2H) IR: 3314, 2954, 1686, 1639, 1543, 1449, 1250, 1059 According to the same procedures, the compounds shown in the following Examples were synthesized.
Example 16 Trans-4-amidino-[(S)-N-[(R)-2-ethoxycarbonylamino=.3-cyclohexylpropanoyl] prolyl]aminoethylcyclohexane (compound No. 227 of Table 1) hydrochloride NMR (DMSO-d6) 8.93 (br, 2H), 8.81 (br, 2H), 7.53 (br, 1 H), 7.38 (t, 1 H), 4.50-4.15 (m, 1 H), 4.10-3.90 (m, 2H), 3.73-3.17 (m, 2H), 3.05-2.80 (m, 3H), 2.39 (br, 1 H), 2.00-0.68 (m, 29H) IR: 3297, 2926, 2853, 1684, 1543, 1449, 1262, 1053 Example 17 Trans-4-amidino-[(S)-N-[(R)-2-isopropoxycarbonylarriino-4,4-dimethylpentanoyl] prolyl]aminomethylcyclohexane (compound No. 265 of Table 1) hydrochloride 'JMR (DMSO-ds) 2140598 8.91 (br, 2H), 8.78 (br, 2H), 7.55 (br, 1 H), 7.28 (t, 1 H), 4.78-4.70 (m, 1 H), 4.30-3.92 (m, 1 H), 3.80-3.20 (m, 3H), 3.0-2.75 (m, 2H), 2.50-1.37 (m, 14H), 1.18-1.00 (m, 6H), 1.0-0.81 (m, 1 H) IR: 3285, 2953, 2870, 1684, 1541, 1449, 1250, 1111 Example 18 Trans-4-amidino-[(S)-N-((R)-N'-methylsulfonylphenylalanyl) prolyl]
aminomethylcyclohexane (compound No. 250 of Table 1) hydrochloride NMR (DMSO-d6) 8.88 (br, 2H), 8.75 (br, 2H), 7.85 (t, 1 H), 7.65 (d, 1 H), 4.27 (m, 1 H), 4.16 (m, 1 H), 3.51-3.41 (m, 4H), 2.99-2.70 (m, 4H), 2.78 (s, 3H), 2.38 (t, 1 H), 1.90-1.40 (m, 9H), 1.08-0.87 (m, 2H) IR: 3375, 2930, 1637, 1452, 1309, 1149, 1097, 983 Example 19 Trans-4-amidino-[(S)-N-((R)-N'-methylsulfonylleucyl) prolyl]
aminomethylcyclohexane (compound No. 269 of Table 1) hydrochloride NMR (DMSO-d6) 8.89 (br, 2H), 8.85 (br, 2H), 6.56 (d, 1 H), 4.53 (m, 1 H), 4.17 (m, 1 H), 3.86 (m, 1 H), 3.47 (m, 1 H), 3.07 (m, 2H), 2.97 (s, 3H), 2.13-1.80 (m, 10H), 1.63-1.54 (m, 4H), 1.33 (m, 1 H), 0.98-0.87 (m, 2H), 0.97 (d, 6H) IR: 3261, 2932, 1639, 1450, 1313, 1143, 1087, 985 Example 20 Trans-4-amidino-[(S)-N-((R)-2-methylsulfonylamino-3-cyclohexyl-propanoyl) prolyl]aminomethylcyclohexane (compound No. 230 of Table 1) hydrochloride NMR (DMSO-d6) 8.95 (br, 2H), 8.53 (br, 2H), 7.27 (m, 1 H), 6.51 (d, 1 H), 4.51 (m, 1 H), 4.19 (m, 1 H), 3.83 (m, 1 H), 3.66 (m, 1 H), 3.41 (m, 2H), 3.04 (m, 2H), 3.04 (m, 2H), 2.95 (s, 3H), 2.46 (t, 1 H), 2.12-0.92 (m, 24H) IR: 3265, 2926, 1639, 1545, 1448, 1315, 1143, 985 Example 21 Trans-4-amidino-[(S)-N-((R)-2-isopropoxycarbonylamino-2-cyclohexylacetyl) prolyl]aminomethylcyclohexane (compound No. 228 of Table 1) hydrochloride NMR (DMSO-d6) 8.91 (br, 2H), 8.69 (br, 2H), 7.36 (br, 1 H), 5.99 (d, 1 H), 4.84-4.79 (m, 1 H), 4.58 (br, 2H), 4.53-4.50 (m, 2H), 4.10-3.90 (m, 2H), 3.60-3.40 (m, 1 H), 2.50-0.97 (m, 30H) IR: 3297, 2980, 2930, 2855, 1684, 1539, 1451, 1258 Example 22 Trans-4-amidino-[(S)-N-((R)-2-ethoxycarbonylamino-4-ethyl-hexanoyl) prolyl]aminomethylcyclohexane (compound No. 264 of Table 1) hydrochloride NMR (DMSO-d6) 8.91 (br, 2H), 8.70 (br, 2H), 7.54 (m, 1 H), 6.34 (m, 1 H), 4.56 (m, 1 H), 4.38 (m, 1 H), 4.11 (m, 3H), 3.48 (m, 1 H), 3.21 (m, 1 H), 2.88 (m, 1 H), 2.68 (m, 1 H), 2.30-1.19 (m, 18H), 1.26 (t, 3H), 0.96 (m, 2H), 0.86 (t, 6H) IR: 3279, 2962, 1685, 1639, 1541, 1448, 1257, 1059, 752 Example 23 Trans-4-amidino-[(S)-N-[(R)-2-t-butoxycarbonylamino-4,4-dimethylpentanoyl] prolyl]aminomethylcyclohexane (compound No. 266 of Table 1) glycolate NMR (DMSO-d6) 9.54 (br, 2H), 8.72 (br, 2H), 7.54 (br, 1H), 7.01 (t, 1H), 4.60-4.00 (m, 4H), 3.40 (m, 2H), 3.10-2.75 (m, 3H), 2.35 (br, 1 H), 2.00-1.20 (m, 24H), 0.91 (s, 9H) IR: 3316, 2953, 1686, 1543, 1449, 1368, 1167 Example 24 4-[(S)-N-[(R)-2-t-butyloxycarbonylamino-cyclohexylai:,etyl] prolyl]
aminomethyl-benzamidoxime (compound No. 396 of Table 1) To a solution of the compound (0.94 g, 2 mmol) obtained in the item (c) of Example 1 in ethanol (15 ml), a solution of sodium carbonate (0.17 g, 1.6 mmol) in water (3 ml) and hydroxyamine hydrochloride (0.22 g, 3.2 mmol) are added. After the reaction mixture is heated at reflux for 8 hours, the solvent is evaporated and the resulting residue is purified with silica gel column chromatography (chloroform-methanol) to give 0.84 g of the titled compound (84%).
Example 16 Trans-4-amidino-[(S)-N-[(R)-2-ethoxycarbonylamino=.3-cyclohexylpropanoyl] prolyl]aminoethylcyclohexane (compound No. 227 of Table 1) hydrochloride NMR (DMSO-d6) 8.93 (br, 2H), 8.81 (br, 2H), 7.53 (br, 1 H), 7.38 (t, 1 H), 4.50-4.15 (m, 1 H), 4.10-3.90 (m, 2H), 3.73-3.17 (m, 2H), 3.05-2.80 (m, 3H), 2.39 (br, 1 H), 2.00-0.68 (m, 29H) IR: 3297, 2926, 2853, 1684, 1543, 1449, 1262, 1053 Example 17 Trans-4-amidino-[(S)-N-[(R)-2-isopropoxycarbonylarriino-4,4-dimethylpentanoyl] prolyl]aminomethylcyclohexane (compound No. 265 of Table 1) hydrochloride 'JMR (DMSO-ds) 2140598 8.91 (br, 2H), 8.78 (br, 2H), 7.55 (br, 1 H), 7.28 (t, 1 H), 4.78-4.70 (m, 1 H), 4.30-3.92 (m, 1 H), 3.80-3.20 (m, 3H), 3.0-2.75 (m, 2H), 2.50-1.37 (m, 14H), 1.18-1.00 (m, 6H), 1.0-0.81 (m, 1 H) IR: 3285, 2953, 2870, 1684, 1541, 1449, 1250, 1111 Example 18 Trans-4-amidino-[(S)-N-((R)-N'-methylsulfonylphenylalanyl) prolyl]
aminomethylcyclohexane (compound No. 250 of Table 1) hydrochloride NMR (DMSO-d6) 8.88 (br, 2H), 8.75 (br, 2H), 7.85 (t, 1 H), 7.65 (d, 1 H), 4.27 (m, 1 H), 4.16 (m, 1 H), 3.51-3.41 (m, 4H), 2.99-2.70 (m, 4H), 2.78 (s, 3H), 2.38 (t, 1 H), 1.90-1.40 (m, 9H), 1.08-0.87 (m, 2H) IR: 3375, 2930, 1637, 1452, 1309, 1149, 1097, 983 Example 19 Trans-4-amidino-[(S)-N-((R)-N'-methylsulfonylleucyl) prolyl]
aminomethylcyclohexane (compound No. 269 of Table 1) hydrochloride NMR (DMSO-d6) 8.89 (br, 2H), 8.85 (br, 2H), 6.56 (d, 1 H), 4.53 (m, 1 H), 4.17 (m, 1 H), 3.86 (m, 1 H), 3.47 (m, 1 H), 3.07 (m, 2H), 2.97 (s, 3H), 2.13-1.80 (m, 10H), 1.63-1.54 (m, 4H), 1.33 (m, 1 H), 0.98-0.87 (m, 2H), 0.97 (d, 6H) IR: 3261, 2932, 1639, 1450, 1313, 1143, 1087, 985 Example 20 Trans-4-amidino-[(S)-N-((R)-2-methylsulfonylamino-3-cyclohexyl-propanoyl) prolyl]aminomethylcyclohexane (compound No. 230 of Table 1) hydrochloride NMR (DMSO-d6) 8.95 (br, 2H), 8.53 (br, 2H), 7.27 (m, 1 H), 6.51 (d, 1 H), 4.51 (m, 1 H), 4.19 (m, 1 H), 3.83 (m, 1 H), 3.66 (m, 1 H), 3.41 (m, 2H), 3.04 (m, 2H), 3.04 (m, 2H), 2.95 (s, 3H), 2.46 (t, 1 H), 2.12-0.92 (m, 24H) IR: 3265, 2926, 1639, 1545, 1448, 1315, 1143, 985 Example 21 Trans-4-amidino-[(S)-N-((R)-2-isopropoxycarbonylamino-2-cyclohexylacetyl) prolyl]aminomethylcyclohexane (compound No. 228 of Table 1) hydrochloride NMR (DMSO-d6) 8.91 (br, 2H), 8.69 (br, 2H), 7.36 (br, 1 H), 5.99 (d, 1 H), 4.84-4.79 (m, 1 H), 4.58 (br, 2H), 4.53-4.50 (m, 2H), 4.10-3.90 (m, 2H), 3.60-3.40 (m, 1 H), 2.50-0.97 (m, 30H) IR: 3297, 2980, 2930, 2855, 1684, 1539, 1451, 1258 Example 22 Trans-4-amidino-[(S)-N-((R)-2-ethoxycarbonylamino-4-ethyl-hexanoyl) prolyl]aminomethylcyclohexane (compound No. 264 of Table 1) hydrochloride NMR (DMSO-d6) 8.91 (br, 2H), 8.70 (br, 2H), 7.54 (m, 1 H), 6.34 (m, 1 H), 4.56 (m, 1 H), 4.38 (m, 1 H), 4.11 (m, 3H), 3.48 (m, 1 H), 3.21 (m, 1 H), 2.88 (m, 1 H), 2.68 (m, 1 H), 2.30-1.19 (m, 18H), 1.26 (t, 3H), 0.96 (m, 2H), 0.86 (t, 6H) IR: 3279, 2962, 1685, 1639, 1541, 1448, 1257, 1059, 752 Example 23 Trans-4-amidino-[(S)-N-[(R)-2-t-butoxycarbonylamino-4,4-dimethylpentanoyl] prolyl]aminomethylcyclohexane (compound No. 266 of Table 1) glycolate NMR (DMSO-d6) 9.54 (br, 2H), 8.72 (br, 2H), 7.54 (br, 1H), 7.01 (t, 1H), 4.60-4.00 (m, 4H), 3.40 (m, 2H), 3.10-2.75 (m, 3H), 2.35 (br, 1 H), 2.00-1.20 (m, 24H), 0.91 (s, 9H) IR: 3316, 2953, 1686, 1543, 1449, 1368, 1167 Example 24 4-[(S)-N-[(R)-2-t-butyloxycarbonylamino-cyclohexylai:,etyl] prolyl]
aminomethyl-benzamidoxime (compound No. 396 of Table 1) To a solution of the compound (0.94 g, 2 mmol) obtained in the item (c) of Example 1 in ethanol (15 ml), a solution of sodium carbonate (0.17 g, 1.6 mmol) in water (3 ml) and hydroxyamine hydrochloride (0.22 g, 3.2 mmol) are added. After the reaction mixture is heated at reflux for 8 hours, the solvent is evaporated and the resulting residue is purified with silica gel column chromatography (chloroform-methanol) to give 0.84 g of the titled compound (84%).
NMR (CDCI3) 1.0-1.49 (m, 14H), 1.5-2.4 (m, 10H), 3.56 (br, 1 H), 3.97 (br, 1 H), 4.09 (t, 1 H), 4.41 (dq, 2H), 4.67 (d, 1 H), 4.94 (br, 2H), 5.41 (d, 1 H), 7.20 (d, 2H), 7.23-7.27 (m, 1 H), 7.50 (d, 2H), 7.75 (br, 1 H) IR: 3345, 2978, 2930, 2855, 1640, 1528, 1449, 1167 According to the same procedures, the compounds shown in the following Examples were synthesized.
Example 25 4-[(S)-N-phenylacetylprolyl] aminomethyl-benzamidoxime (compound No. 374 of Table 1) NMR (CDCI3) 8.11 (t, 1 H), 7.37 (d, 2H), 7.28-7.23 (m, 5H), 7.08 (d, 2H), 4.88 (s, 2H), 4.68 (d, 1 H), 4.51 (m, 1 H), 4.21 (m, 1 H), 3.71 (s, 2H), 3.63-3.51 (m, 2H), 2.40-2.01 (m, 4H) IR: 3315, 2968, 1637, 1543, 1244, 1155, 927, 709 Example 26 4-[(S)-N-[(R)-N'-ethoxycarbonylphenylalanyl] prolyl]aminomethyl-benzamidoxime (compound No. 387 of Table 1) NMR (CDCI3) 7.54 (d, 2H), 7.27-7.19 (m, 7H), 6.31 (d, 1 H), 5.05 (br, 2H), 4.65-4.42 (m, 3H), 4.24-4.10 (m, 1 H), 3.80-3.40 (m, 3H), 3.10-2.95 (m, 2H), 2.60-2.50 (m, 1 H), 2.14 (br, 1 H), 1.95-1.50 (m, 3H), 0.99 (t, 3H) IR: 3339, 1641, 1539, 1451, 1260, 752, 702 ~ ~~:
Example 27 4-[(S)-N-[(R)-2-t-butyloxycarbonylamino-3-cyclohexylpropanoyl]
prolyl]aminomethyl-benzamidoxime (compound No. 397 of Table 1) NMR (CDCI3) 7.75 (br, 1 H), 7.50 (d, 2H), 7.21 (d, 2H), 5.40 (d, 1 H), 4.94 (br, 2H), 4.64 (br, 1 H), 4.40-4.25 (m, 3H), 3.95 (br, 1 H), 3.50-3.40 (m, 1 H), 2.0-0.80 (m, 26H) IR: 3337, 2978, 2924, 2851, 1642, 1536, 1449, 1167 Example 28 4-[(S)-N-[(R)-2-ethoxycarbonylamino-3-methyl-3-methylthiobutanoyl]
prolyl]aminomethyl-benzamidoxime (compound No. 419 of Table 1) NMR (CDCI3) 7.66 (t, 1 H), 7.53 (d, 2H), 7.23 (d, 2H), 5.64 (d, 1 H), 4.91 (s, 2H), 4.68 (d, 1 H), 4.58-4.30 (m, 3H), 3.90 (m, 1 H), 3.87-3.76 (m, 2H), 3.62 (m, 1 H), 2.37 (m, 1 H), 2.09-2.00 (m, 3H), 2.06 (s, 3H), 1.41 (s, 3H), 1.39 (s, 3F1), 1.09 (t, 3H) IR: 3339, 2978, 1641, 1535, 1439, 1249, 1057, 929, 754 Example 29 4-[(S)-N-[(R)-phenyialanyl] prolyl]aminomethyl-benzamidoxime (compound No. 390 of Table 1) dihydrochloride NMR (DMSO-d6) 11.24 (br, 1 H), 9.02 (br, 2H), 8.91 (t, 1 H), 8.80 (br, 3H), 7.66 (d, 2H), 7.44 (d, 2H), 7.35-7.22 (m, 5H), 4.30-4.16 (m, 4H), 3.57-2.95 (m, 3H), 2.45-2.30 (m, 1 H), 1.90-1.20 (m, 4H) IR: 3059, 1649, 1539, 1491, 1454 Example 30 Trans-4-[(S)-N-((R)-2-isopropoxycarbonylamino-2-(:yclohexylacetyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 430 of Table 1) NMR (CDCI3) 7.14 (br, 1 H), 5.70 (d, 1 H), 4.85-4.80 (m, 1 H), 4.70 -4.50 (m, 3H), 4.17-4.08 (m, 2H), 3.96 (br, 1 H), 3.54 (q, 1 H), 3.05 (t, 2H), 2.40-,":'..20 (m, 1 H), 2.09-0.88 (m, 30H) IR: 3342, 2978, 2928, 2855, 1653, 1449, 1256, 1111 Example 31 Trans-4-[(S)-N-((R)-2-t-butoxycarbonylamino-3-cyclohexylpropanoyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 435 of Table 1) NMR (CDCI3) 7.14 (br, 1 H), 5.40 (d, 1 H), 4.60-4.33 (m, 5H), 3.88 (br, 1 H), 3.43 (q, 1 H), 3.20-3.11 (m, 1 H), 3.0-2.96 (m, 1 H), 2.40-2.30 (m, 1 H), 2.0-0.84 (m, 35H) IR: 3356, 2926, 2853, 1649, 1537, 1448, 1167 Example 32 Trans-4-[(S)-N-((R)-2-t-butoxycarbonylamino-2-cyclohexylacetyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 433 of Table 1) NMR (CDCI3) 7.15 (br, 1 H), 5.28 (d, 1 H), 4.58 (br, 4H), 4.09 (t, 1 H), 3.92 (br, 1 H), 3.53 (q, 1 H), 3.20-2.90 (m, 2H), 2.40 (br, 1 H), 2.10-0.91 (m, 33H) IR: 3347, 2930, 2855, 1649, 1541, 1451, 1169 Example 33 Trans-4-[(S)-N-[(R)-2-t-ethoxycarbonylamino-4,4-dirriethylpentanoyl]
prolyl]aminomethylcyclohexanecarboxamidoxime (compourid No. 461 of Table 1) NMR (CDCI3) 7.06 (t, 1 H), 5.56 (d, 1 H), 4.57-4.39 (m, 4H), 4.11 (q, 2H), 3.98 (m, 1 H), 3.47 (m, 1 H), 3.05 (m, 2H), 2.39 (m, 1 H), 2.04-1.78 (m, 10H), 1.57 (d, 2H), 1.56-1.12 (m, 2H), 1.24 (t, 3H), 0.99 (s, 9H), 0.99-0.89 (m, 2H) IR: 3356, 2934, 1649, 1541, 1446, 1249, 1059, 927 Example 34 Trans-4-[(S)-N-[(R)-2-methoxycarbonylamino-4,4-dinnethylpentanoyl]
prolyl]aminomethylcyclohexanecarboxamidoxime (compourid No. 458 of Table 1) <~
NMR (CDCI3) 7.04 (t, 1 H), 5.53 (d, 1 H), 4.68 (s, 2H), 4.56 (d, 1 H), 4.43 (m, 1 H), 3.98 (m, 1 H), 3.66 (s, 3H), 3.47 (m, 1 H), 3.07 (m, 2H), 2.39 (m, 1 H), 2.19-1.77 (m, 8H), 1.57 (d, 2H), 1.55-1.25 (m, 4H), 0.99 (s, 9H), 0.93 (m, 2H) IR: 3344, 2949, 1712, 1649, 1548, 1448, 1249, 1059 Example 35 Trans-4-[(S)-N-[(R)-2-t-butoxycarbonylamino-4,4-dirnethylpentanoyl]
prolyl]aminomethylcyclohexanecarboxamidoxime (compourid No. 467 of Table 1) NMR (CDCI3) 7.12 (t, 1 H), 5.14 (d, 1 H), 4.58 (d, 1 H), 4.53 (s, 2H), 4.37 (m, 1 H), 3.92 (m, 1 H), 3.45 (m, 1 H), 3.19 (m, 1 H), 2.95 (m, 1 H), 2.42 (m, 1 H), 2.06-1.79 (m, 8H), 1.53 (d, 2H), 1.52-1.34 (m, 4H), 1.43 (s, 9H), 0.99 (s, 9H), 1.00-0.89 (m, 2H) IR: 3358, 2930, 1649, 1535, 1448, 1367, 1249, 1168 Example 36 Trans-4-[(S)-N-[(R)-2-benzyloxycarbonylamino-4,4-dimethylpentanoyl]
prolyl]aminomethylcyclohexanecarboxamidoxime (compourid No. 469 of Table 1) NMR (CDCig) 7.36-7.27 (m, 5H), 7.04 (t, 1 H), 5.63 (d, 1 H), 5.16-5.00 (m, 2H), 4.58-4.46 (m, 4H), 3.97 (m, 1 H), 3.47 (m, 1 H), 3.06-2.92 (m, 2H), 2.43-2.38 (m, 1 H), 2.01-1.72 (m, 8H), 1.58 (d, 2H), 1.50-1.23 (m, 4H), 0.98 (s, 9H), 0.98-0.88 (m, 2H) IR: 3356, 2928, 1649, 1541, 1448, 1249, 1053 929 Example 37 Trans-4-[(S)-N-[(R)-2-isopropoxycarbonylamino-4,4-dimethylpentanoyl]
prolyl] aminomethylcyclohexanecarboxamidoxime (compoiund No. 464 of Table 1) NMR (CDCI3) 7.11 (t, 1 H), 5.49 (d, 1 H), 4.83 (m, 1 H), 4.56 (m, 3H), 4.42 (dd, 1 H), 3.98 (m, 1 H), 3.47 (dd, 1 H), 3.04 (m, 2H), 2.40 (m, 1 H), 2.01 (m, 2H), 1.92 (m, 3H), 1.80 (m, 3H), 1.57 (d, 2H), 1.39 (m, 4H), 1.21 (m, 6H), 0.99 (s, 9H), 0.94 (m, 2H) IR: 3343, 1649, 1541, 1449, 1275 Example 38 Trans-4-[(S)-N-[(R)-2-isopropoxycarbonylamino-2-cyclopentylacetyl]
prolyl]aminomethylcyclohexanecarboxamidoxime (compourid No. 464 of Table 1) NMR (CDCI3) 7.14 (t, 1 H), 5.42 (d, 1 H), 4.83 (m, 1 H), 4.60 (d, 1 H), 4.52 (s, 2H), 4.13 (m, 1 H), 3.98 (m, 1 H), 3.56 (m, 1 H), 3.04 (m, 2H), 2.35 (m, 1 H), 2.24 (m, 1 H), 2.10-1.30 (m, 20H), 1.23 (dd, 6H), 1.01-0.93 (m, 2H) IR: 3344, 2934, 1649, 1541, 1448, 1275, 1111, 754 Example 39 Trans-4-[(S)-N-((R)-2-t-butoxycarbonylamino-2-cyclopentylacetyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 432 of Table 1) NMR (CDCI3) 7.16 (t, 1 H), 5.16 (d, 1 H), 4.60 (d, 1 H), 4.51 (s, 2H), 4.14 (t, 1 H), 3.94 (m, 1 H), 3.52 (m, 1 H), 3.01 (m, 2H), 2.38 (m, 1 H), 2.23-1.39 (mõ 21 H), 1.43 (s, 9H), 1.17-0.90 (m, 2H) IR: 3350, 2932, 1649, 1541, 1448, 1367, 1251, 1167, 929 Example 40 Trans-4-[(S)-N-((R)-2-ethoxycarbonylamino-3-cyclohexylpropanoyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 428 of Table 1) NMR (CDCI3) 7.08 (br, 1 H), 5.53 (d, 1 H), 4.80-4.40 (m, 4H), 4.10-3.85 (m, 4H), 3.44 (q, 1 H), 3.06 (t, 3H), 2.15-0.90 (m, 29H) IR: 3343, 2926, 2853, 1649, 1541, 1449, 1260, 1053 Example 41 Trans-4-[(S)-N-((R)-2-isopropoxycarbonylamino-3-cyclohexyl-propanoyl) prolyl] aminomethylcyclohexanecarboxamidoxirne (compound No. 431 of Table 1) NMR (CDCI3) 7.12 (br, 1 H), 5.51 (d, 1 H), 4.85-4.70 (m, 1 H), 4.60-4.30 (m, 4H), 4.0-3.85 (m, 1 H), 3.44 (q, 1 H), 3.10-2.95 (m, 3H), 2.45-2.35 (m, 1 H), 2.05-0.80 (m, 32H) IR: 3347, 2978, 2926, 2853, 1649, 1539, 1449, 1261, 1111 214 059 8 _ Example 42 Trans-4-[(S)-N-((R)-2-isopropoxycarbonylamino-4-ethyl-hexanoyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 463 of Table 1) NMR (CDCI3) 7.11 (t, 1 H), 5.41 (d, 1 H), 4.83 (m, 1 H), 4.56 (m, 3H), 4.39 (m, 1 H), 3.94 (m, 1 H), 3.46 (m, 1 H), 3.02 (m, 2H), 2.39 (m, 1 H), 2.10-1.20 (m, 20H), 1.22 (dd, 6H), 1.02-0.84 (m, 2H), 0.86 (t, 6H) IR: 33346, 2962, 2930, 1653, 1541, 1448, 1271, 1113 Example 43 Trans-4-[(S)-N-((R)-2-t-butoxycarbonylamino-4-ethyl-hexanoyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 466 of Table 1) NMR (CDCI3) 7.19 (t, 1 H), 5.14 (d, 1 H), 4.60 (d, 1 H), 4.50 (s, 2H), 433 (m, 1 H), 3.89 (m, 1 H), 3.43 (m, 1 H), 3.15 (m, 1 H), 2.95 (m, 1 H), 2.40 (m, 1 H), 2.10-1.19 (m, 20H), 1.43 (s, 9H), 1.04-0.89 (m, 2H), 0.86 (t, 6H) IR: 3346, 2964, 2930, 1649, 1541, 1448, 1367, 1280, 1251, 1168, 929 Example 44 Trans-4-[(S)-N-((R)-2-ethoxycarbonylamino-heptanoyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 459 of Table 1) `~.
,,. A. .
NMR (CDCI3) 7.08 (t, 1 H), 5.60 (d, 1 H), 4.58 (m, 3H), 4.35 (m, 1 H), 4.07 (m, 2H), 3.92 (m, 1 H), 3.48 (m, 1 H), 3.06 (m, 2H), 2.40 (m, 1 H), 2.04-1.32 (m, 20H), 1.24 (t, 3H), 0.89 (t, 3H), 0.98 (m, 2H) I R: 3346, 2928, 1649, 1541, 1448, 1255, 1055, 927 Example 45 Trans-4-[(S)-N-((R)-N'-t-butoxycarbonylamino-methionyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 468 of Table 1) NMR (CDCI3) 7.07 (m, 1 H), 5.31 (d, 1 H), 4.55 (m, 4H), 3.56 (m, 1 H), 3.10 (m, 2H), 2.57 (t, 2H), 2.37 (m, 1 H), 2.11 (s, 3H), 2.06-1.29 (m, 14H), 1.43 (s, 9H), 1.00 (m, 2H) IR: 3354, 2928, 1647, 1541, 1448, 1367, 1251, 1167 Example 46 Trans-4-[(S)-N-((R)-2-hydroxy-4,4-dimethyl-pentanoyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 454 of Table 1) NMR (CDCI3) 7.19 (t, 1 H), 4.68 (s, 2H), 4.50 (d, 1 H), 4.36 (t, 1 H), 3.64 (t, 1 H), 3.39 (m, 1 H), 3.06 (m, 2H), 2.35 (m, 2H), 2.16-1.79 (m, 9H), 1.44 (d, 2H), 1.43-1.25 (m, 3H), 1.00-0.95 (m, 2H), 1.02 (s, 9H) IR: 3337, 2944, 1653, 1620, 1566, 1448, 1386, 1248; 1087' '*~.
Example 47 Trans-4-[(S)-N-((R)-2-ethoxycarbonylamino-4-ethyl-hexanoyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 460 of Table 1) NMR (CDCI3) 7.07 (t, 1 H), 5.53 (d, 1 H), 4.56 (m, 3H), 4.40 (m, 1 H), 4.11 (q, 2H), 3.96 (m, 1 H), 3.45 (m, 1 H), 3.05 (m, 2H), 2.36 (m, 1 H), 2.09-1.7"d' (m, 10H), 1.61-1.21 (m, 8H), 1.24 (t, 3H), 1.02-0.83 (m, 2H), 0.86 (t, 6H) IR: 3342, 2962, 2930, 1649, 1541, 1448, 1379, 1269, 1059, 929 Example 48 Trans-4-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl]
prolyl] aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 531 of Table 1) To a solution of the compound (4.2 g, 8.9 mmol) obtained in Example 33 and triethylamine (1.9 ml, 13.3 mmol) in dichloromethane (100 ml), a solution of methyl chloroformate (1.0 g, 10 mmol) in dichloromethane (10 ml) is added at O'C. After stirring for 4 hours, the organic layer is washed once with an aqueous saturated sodium bicarbonate solution, water and saturated brine, successively. After drying over sodium sulfate, the solvent is evaporated and the residue is purified with silica gel column chromatography (ethyl acetate-methanol) to give 2.9 g of the titled compound (62%).
NMR (CDCI3) 0.89-1.07 (m, 11 H), 1.21-1.60 (m, 8H), 1.79-2.40 (m, 9H), 3.0-3.10 (m, 2H), 3.40-3.50 (m, 1 H), 3.84 (s, 3H), 3.84-4.20 (m, 3H), 4.35-4.40 (m, 1 H), 4.55 i`:~
(d, 1 H), 4.81 (br, 2H), 5.19 (d, 1 H), 7.12 (t, 1 H) IR: 3345, 2953, 1763, 1699, 1645, 1541, 1443, 1256 According to the same procedures, the compounds shown in the following Examples were synthesized.
Example 49 4-[(S)-N-((R)-2-hydroxy-2-cyclohexylacetyl) prolyl]arninomethyl-benzamide O-ethoxycarbonyloxime (compound No. 543 of Table 1) NMR (CDCI3) 7.56 (d, 2H), 7.47 (t, 1 H), 7.22 (d, 2H), 5.35 (s, 2H), 4.53 (m, 2H), 4.37 (d, 2H), 4.30 (q, 2H), 4.07 (m, 1 H), 3.64 (m, 1 H), 3.47 (m, 1 H), 3.39 (m, 1 H), 2.35-1.17 (m, 15H), 1.35 (t, 3H) IR: 3368, 2928, 1772, 1628, 1554, 1452, 1404, 1228, 1087, 856 Example 50 Trans-4-[(S)-N-((R)-2-hydroxy-4,4-dimethylpentanoyl) prolyl]
aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 534 of Table 1) NMR (CDCI3) 7.07 (t, 1 H), 4.77 (s, 2H), 4.52 (d, 1 H), 4.34 (m, 1 H), 3.85 (s, 3H), 3.58 (t, 1 H), 3.37 (m, 1 H), 3.22 (d, 1 H), 3.12-3.05 (m, 2H), 2.26-2.21 (m, 1 H), 1.97-1.37 (m, 13H), 1.03 (s, 9H), 1.09-0.95 (m, 2H) IR: 3346, 2953, 1763, 1643, 1442, 1257, 1089, 879 Example 51 Trans-4-[(S)-N-((R)-2-hydroxy-4,4-dimethylpentanoyl)prolyl]
aminomethylcyclohexanecarboxamide O-ethoxycarbonyloxime (compound No. 556 of Table 1) NMR (CDCI3) 7.05 (t, 1 H), 4.73 (s, 2H), 4.52 (d, 1 H), 4.34 (t, 1 H), 4.27 (q, 2H), 3.58 (m, 1 H), 3.45 (m, 1 H), 3.08 (m, 2H), 2.44 (m, 1 H), 2.30-1.30 (m, 13H), 1.32 (t, 3H), 1.03 (s, 9H), 1.07-0.92 (m, 2H) IR: 3373, 2953, 1759, 1641, 1450, 1369, 1248, 1093 Example 52 Trans-4-amino-[(S)-N-[(R)-N'-methanesulfonylphenyPalanyl] prolyl]
aminomethylcyclohexane (compound No. 776 of Table 1) L-tartrate.
(a) Trans-4-t-butyloxycarbonylamino-benzyloxycarbonylamino--methylcyclohexane To a solution of trans-4-aminomethylcyclohexanecarboxylic acid (15.7 g, 100 mmol) and sodium hydroxide (4.0 g, 100 mmol) in water (30 ml), benzyloxycarbonyl chloride (15.6 ml, 110 mmol) and sodiurn hydroxide (4.4 g, 110 mmol) in water (30 ml) are added dropwise at 0 C, simultaneously. After stirring for 4 hours, the mixture is extracted once with ether and 1 N-hydrochloric acid is added to the aqueous layer until the pH of the mixture indicates 2. Then, the precipitated white solid is collected and dried.
To a solution of the resulting compound (12.8 g, 50 nimol) in t-butanol (150 ml), triethylamine (8.3 ml, 60 mmol) and DPPA (13.7 g, 50 mmol) are ~~.
~' .
2f40598 added and heated at reflux for 8 hours. After the solvent is evaporated, water is added to the residue and the mixture is extracted with chloroform. The organic layer is washed once with an aqueous sodium carbonate (5%), once with an aqueous potassium hydrogensulfate (5%), twice with water and once with saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the residue is purified with silica gel column chromatography (hexane-ethyl acetate) to give 8.6 g of the titled compound (47%).
NMR (CDCI3) 0.85-1.37 (m, 14H), 1.60-1.85 (m, 4H), 2.84 (t, 1 H), 3.12 (br, 1 H), 5.00 (s, 2H), 6.62 (d, 1 H), 7.23-7.39 (m, 6H) (b) Trans-4-t-butyloxycarbonylamino-[(S)-N-benzyloxycarbonylprolylJ
aminomethylcyclohexane The compound (4.4 g, 12 mmol) obtained in the item (a) is dissolved in methanol (200 ml) and the catalytic hydrogenation is conducted at room temperature and under atomospheric pressure in the presence of palladium black (0.4 g). After the completion of the reaction, the catalyst is filtered off and the solvent is evaporated.
To a solution of (S)-Z-proline (3.0 g, 12 mmol) in THF (30 ml), CDI (2.0 g, 12 mmol) is added at 0 C. After stirring for 3 hours, a solution of the compound obtained in the above reaction in THF (150 ml) is added at 0 C. After stirring for 6 hours, the solvent is evaporated and water (50 ml) is added to the residue.
The mixture is extracted with chloroform and the organic layer is washed three 2140598 _ times with water and once with saturated brine, successively. After drying over sodium sulfate, the solvent is evaporated and the residue is purified with silica gel chromatography (chloroform-methanol) to give 4.2 g of the titled compound (77%).
NMR (CDCI3) 0.85-1.06 (m, 4H), 1.44 (s, 9H), 1.60-2.35 (m, 9H), 2.94-3.20 (m, 2H), 3.20-3.55 (m, 3H), 4.31 (br, 1 H), 4.47 (br, 1 H), 5.14 (s, 2H), 6.90 (br, 1 H), 7.15-7.40 (m, 5H) (c) Trans-4-t-butyloxycarbonylamino-[(S)-N-[(R)-N'-benzyloxycarbonylphenylalanyl] prolyl] aminomethylcyclohexane The compound (3.6 g, 7.9 mmol) obtained in the item (b) is dissolved in methanol (50 ml) and the catalytic hydrogenation is conducted at room temperature and under atomospheric pressure in the presence of palladium black (0.3 g). After the completion of the reaction, the catalyst is filtered off and the solvent is evaporated.
To a solution of (R)-Z-phenylalanine (2.4 g, 7.9 mmol) in THF (30 ml), CDI (1.3 g, 7.9 mmol) is added at O'C. After stirring for 4 hours, a solution of the compound obtained in the above reaction in THF (60 ml) is added. After stirring for 8 hours, the solvent is evaporated and water is added to the reaction mixture. The mixture is extracted with chloroform and the organic layer is washed three times with water and once with saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the residue is purified with silica gel column chromatography (chloroforrn-methanol) to give J'" '.
4.2 g of the titled compound (89%).
NMR (CDCI3) 0.85-1.06 (m, 5H), 1.33-2.0 (m, 15H), 2.10-2.22 (m, '1 H), 2.50-2.60 (m, 1 H), 2.94-3.01 (m, 5H), 3.30 (br, 1 H), 3.57 (t, 1 H), 4.32-4.59 (m, 3H), 5.08 (d, 2H), 5.69 (d, 1 H), 7.02 (br, 1 H), 7.18-7.37 (m, 10H) (d) Trans-4-amino-[(S)-N-[(R)-N'-methanesulfonylphenylalanyl]prolyl]
aminomethylcyclohexane L-tartrate.
The compound (2.4 g, 3.9 mmol) obtained in the iteni (c) is dissolved in methanol (40 ml) and the catalytic hydrogenation is conducted at room temperature and under atomospheric pressure in the presence of palladium black (0.2 g). After the completion of the reaction, the catalyst is filtered off and the solvent is evaporated. To a solution of the resulting compound in dichloromethane (40 ml), triethylamine (0.65 nnl, 4.7 mmol) is added and a solution of methanesulfonyl chloride (0.47 g, 4.1 mmol) in dichloromethane (100 ml) is further added at 0 C. After stirring for 3 hours, an aqueous saturated sodium bicarbonate solution is added and the organic layer is washed once with water and saturated brine, successively. After drying over sodium sulfate, the solvent is evaporated and the residue is purified with silica gel chromatography (chloroform-methanol).
The resulting compound is dissolved in chloroform (10 ml) and a 4N-dioxane hydrochloride in dioxane (10 ml) is added at 0 C. After stirring for 2 hours, the solvent is evaporated and chloroform (10 ml) and a 1 N-sodium hydroxide solution (10 ml) are added to the residue and, further, the mixture is stirred for 10 minutes. The organic layer is dried over sodium sulfate and a solution of L-tartaric acid (0.34 g, 2.26 nm) in methanol (5 rnl) is added.
The solvent is evaporated and ether (20 ml) is added, and then the precipitated white solid is collected and dried to give 1.36 g of the titled compound (58%).
NMR (DMSO-d6) 7.77 (m, 4H), 7.28 (m, 5H), 4.28 (m, 1 H), 4.16 (m, 1 H), 3.57-3.45 (m, 8H), 2.73 (s, 3H), 1.91-1.75 (m, 9H), 1.54 (m, 1 H), 1.25 (m, 4H), 0.93 (m, 2H) IR: 3324, 2934, 1734, 1638, 1545, 1453, 1308, 1148 According to the same procedures, the compounds shown in the following Examples were synthesized.
Example 53 Trans-4-amino-[(S)-N-[(R)-2-methylsulfonylamino-2-cyclohexylacetyl]
prolyl]aminomethylcyclohexane (compound No. 759 of Table 1) hydrochloride NMR (DMSO-d6) 8.09 (br, 3H), 7.80 (t, 1 H), 7.39 (d, 1 H), 4.30-4.26 (m, 1 H), 3.87 (t, 1 H), 3.80-3.45 (m, 2H), 3.0-2.80 (m, 3H), 2.85 (s, 3H), 2.10-0.80 (m, 24H) IR: 3382, 2930, 2857, 1638, 1543, 1451, 1154 Example 54 Trans-4-amino-[(S)-N-[(S)-N'-benzenesulfonyl-a-glutamyl] prolyl]
aminomethylcyclohexane (compound No. 792 of Table 1) hydrochloride NMR (DMSO-d6) 8.04 (br, 3H), 7.75-7.50 (m, 5H), 4.05 (q, 1 H), 3.77-3.30 (m, 5H), 3.0-2.70 (m, 3H), 2.28 (t, 2H), 2.0-1.52 (m, 10H), 1.31-1.11 (m, 3H), 1.0-0.85 (m, 2H) IR: 3400, 2937, 1637, 1449, 1161 Example 55 Trans-4-amino-[(S)-N-((RS)-3-methylsulfonylamino==3-phenylpropanoyl) prolyl]aminomethylcyclohexane (compound No. 777 of Table 1) hydrochloride NMR (DMSO-d6) 8.08 (m, 3H), 7.34 (m, 5H), 4.78 (m, 1 H), 4.15 (m, 2H), 3.51 (m, 1 H), 3.36 (m, 2H), 2.86 (m, 4H), 2.68 (s, 3H), 2.51 (m, 2H), 2.00-1.69 (m, 6H), 1.27 (m, 4H), 0.92 (m, 2H) IR: 3409, 2936, 1638, 1453, 1314, 1148 Example 56 Trans-4-amino-[(S)-N-((R)-2-isopropoxycarbonylamino-4,4-dimethylpentanoyl) prolyi]aminomethylcyclohexane (compound No. 797 of Table 1) NMR (CDCI3) 7.19 (m, 1 H), 5.32 (d, 1 H), 4.82 (m, 1 H), 4.53 (m, 2H)õ 4.00 (m, 1 H), 3.48 (m, 1 H), 3.03-2.16 (m, 6H), 2.00-1.81 (m, 6H), 1.57 (d, 2H), 1.49 (m, 4H), 1.24 (m, 6H), 1.00 (s, 9H), 0.95 (m, 2H) IR: 3326, 2949, 1640, 1541, 1449, 1248 Example 57 Trans-4-amino-[(S)-N-((R)-N'-ethoxycarbonyl-phenylalanyl) prolyl]
aminomethylcyclohexane (compound No. 780 of Table 1) hydrochloride NMR (DMSO-d6) 7.98 (m, 3H), 7.37 (t, 1 H), 7.26 (m, 5H), 4.37 (dd, 1 H), 4.16 (m, 1 H), 4.02 (m, 2H), 3.88 (m, 1 H), 3.59 (m, 1 H), 3.43 (m, 1 H), 2.86 (m, 5H), 1.93-1.75 (m, 7H), 1.28 (m, 4H), 1.15 (t, 3H), 0.92 (m, 2H) ( R: 3349, 2936, 1642, 1537, 1451, 1258 Example 58 Trans-4-amino-[(S)-((R)-phenylalanyl) prolyl]aminorriethylcyclohexane (compound No. 779 of Table 1) hydrochloride NMR (DMSO-d6) 8.69 (br, 3H), 8.09 (br, 4H), 7.37-7.20 (m, 5H), 4.19 (br, 1 H), 4.09-4.06 (m, 1 H), 3.20-2.82 (m, 5H), 2.0-0.85 (m, 15H) IR: 3426, 2936, 1649, 1539, 1497, 1454 Example 59 Trans-4-amino-[(S)-N-((R)-2-ethoxycarbonyloxy-3-phenylpropanoyl) prolyl]aminomethylcyclohexane (compound No. 785 of Table 1) hydrochloride NMR (DMSO-d6) 7.78 (m, 3H), 7.30 (m, 5H), 7.15 (d, 1 H), 5.22 (t, 1 H), 4.20 (m, 1 H), 4.08 (m, 3H), 3.64 (m, 1 H), 3.02-2.88 (m, 5H), 1.92-1.72 (m, 7H), 1.20-0.94 (m, 9H) IR: 3397, 2938, 1740, 1655, 1453, 1269 Example 60 Trans-4-amino-[(S)-N-((R)-2-allylcarbamoyloxy-3-phenylpropanoyl) prolyl]aminomethylcyclohexane (compound No. 787 of Table 1) hydrobromide NMR (DMSO-d6) 7.90 (m, 3H), 7.30 (m, 5H), 7.14 (m, 1 H), 5.72 (m, 2HI), 5.06 (m, 2H), 4.76 (m, 1 H), 4.17 (m, 1 H), 3.60 (m, 1 H), 2.98-2.85 (m, 5H), 1.87-1.70 (m, 7H), 1.23 (m, 7H), 0.90 (m, 2H) IR: 3364, 2936, 1707, 1645, 1543, 1454, 1256 Example 61 Trans-4-amino-[(S)-N-((R)-2-hydroxy-2-cyclohexylacetyl) prolyl]
aminomethylcyclohexane (compound No. 768 of Table 1) hydrochloride NMR (DMSO-d6) 8.21 (br, 3H), 7.95 (m, 1 H), 4.53 (m, 1 H), 4.18 (d, 1 H), 3.95 (m, 1 H), 3.07 (m, 3H), 2.18-1.55 (m, 22H), 1.30-1.03 (m, 2H) IR: 3422, 2928, 2854, 1637, 1450, 1388, 1240, 1114, 1045 Example 62 Trans-4-amino-[(S)-N-((R)-2-hydroxy-2-phenylacetyl) prolyl]
aminomethylcyclohexane (compound No. 783 of Table 1) hydrochloride :~.
NMR (DMSO-ds) 2 14059 8 7.98 (br, 3H), 7.37-7.28 (m, 5H), 5.48 (br, 1 H), 5.23 (id, 1 H), 4.23 (d, 1 H), 3.70-3.35 (m, 2H), 3.0-2.80 (m, 4H), 2.0-1.60 (m, 8H), 1.40-0.90 (m, 5H) IR: 3329, 2935, 1667, 1626, 1552, 1448 Example 63 Trans-4-amino-[(RS)-1-((R)-N'-methylsulfonyi-phenylalanyl)-2-piperidinecarboxyl]aminomethylcyclohexane (compound No. 834 of Table 1) hydrochloride NMR (DMSO-d6) 8.07 (m, 3H), 7.28 (m, 5H), 4.64 (m, 1 H), 4.39 (m, 1 H), 3.99 (m, 1 H), 3.67 (m, 1 H), 2.87 (m, 7H), 2.84 (s, 3H), 1.91-1.68 (m, 5H), 1.33-0.92 (m, 10H) IR: 3385, 2936, 1638, 1535, 1453, 1314, 1150 Example 64 Trans-4-amino-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl] prolyl]aminomethylcyclohexane (compound No. 794 of Table 1) NMR (CDCI3) 7.16 (m, 1 H), 5.68 (d, 1 H), 4.53 (d, 1 H), 4.38 (m, 1 H), 4.10 (q, 2H), 4.01 (m, 1 H), 3.46-3.07 (m, 4H), 2.30-1.81 (m, 8H), 1.58 (m, 5H), 1.26 (t, 3H), 1.00 (s, 9H), 0.95 (m, 2H) I R: 3329, 2949, 1642, 1541, 1447, 1248, 1059 ,rw Example 65 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl] prolyl]aminornethylcyclohexane (compound No. 968 of Table 1) To a solution of the compound (5.4 g, 11.7 mmol) obtained in Example 64 in DMF (40 ml), sodium carbonate (3.2 g, 23.4 mmol) is added, and a solution of 4-bromomethyl-5-methyl-1,3-dioxo-2-on (4.0 g, 17.6 mmol) in DMF
(5 ml) is further added at 0 C. After stirring for 48 hours, the solvent is evaporated and water is added to the residue, which is extracted with ethyl acetate. The organic layer is washed three times with water and once with saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the residue is purified with silica gel column chromatography (chloroform-methanol) to give 2.8 g of the titled compound (44%).
NMR (CDCI3) 7.07 (m, 1 H), 5.15 (d, 1 H), 4.56 (d, 1 H), 4.41 (m, 1 H), 4.10 (q, 2H), 4.00 (m, 2H), 3.48 (s, 2H), 3.45 (m, 2H), 3.04 (t, 1 H), 2.62 (m, 1 H), 2.38 (m, 1 H), 2.11 (s, 3H), 2.00 (m, 3H), 1.82 (m, 2H), 1.73-1.43 (m, 4H), 1.28 (1:, 3H), 1.26 (m, 3H), 1.00 (s, 9H), 0.96 (m, 2H) IR: 3329, 2934, 2870, 1823, 1649, 1539, 1445, 1223 According to the same procedures, the compounds shown in the following Examples were synthesized.
Example 66 Trans-4-t-butoxycarbonylamino-[(S)-N-[(R)-N'-methanesulfonyl-~, ~~..~
~~ ';~I~
2140598 .
phenylalanyl] prolyl]aminomethylcyclohexane (compound No. 955 of Table 1) NMR (CDCI3) 7.29 (m, 3H), 7.24 (m, 2H), 6.67 (t, 1 H), 5.61 (d, 1 H), 4.40 (m, 2H), 4.29 (dd, 1 H), 3.58 (m, 1 H), 3.34 (m, 1 H), 2.99 (m, 4H), 2.82 (s, 3H), 2.69 (m, 1 H), 2.18-1.74 (m, 9H), 1.43 (s, 9H), 1.02 (m, 4H) IR: 3376, 2932, 1655, 1526, 1453, 1322 Example 67 Trans-4-guanidino-[(S)-N-[(R)-N'-methanesulfonylphenylalanyl) prolyl]aminomethylcyclohexane (compound No. 646 of Table 1) sulfate To a solution of the compound (0.45 g, 1 mmol) obtained in Example 52 in ethanol (15 mi), a solution of 2-methylisothiourea sulfate (0.14 g, 0.5 mmol) in water (5 ml) is added and heated at reflux for 6 hours. Ttie solvent is evaporated and ether (20 ml) is added. The precipitated white solid is collected and washed with ether, and then dried under reduced pressure to give 0.44 g of the titled compound (81 %).
NMR (DMSO-d6) 8.04-2.0 (m, 13H), 2.60-3.96 (m, 7H), 2.77 (s, 3H), 4.14-4.28 (m, 2H), 5.47 (br, 1 H), 6.75 (br, 1 H), 7.20-7.36 (m, 5H), 7.83 (br, 1 H), 8.40 (br, 4H) IR: 3322, 2932, 2193, 2153, 1644, 1545, 1451, 1319, 1150 According to the same procedure as that described iri Example 1, the following compounds of Examples 68 to 78 were synthesized.
Example 25 4-[(S)-N-phenylacetylprolyl] aminomethyl-benzamidoxime (compound No. 374 of Table 1) NMR (CDCI3) 8.11 (t, 1 H), 7.37 (d, 2H), 7.28-7.23 (m, 5H), 7.08 (d, 2H), 4.88 (s, 2H), 4.68 (d, 1 H), 4.51 (m, 1 H), 4.21 (m, 1 H), 3.71 (s, 2H), 3.63-3.51 (m, 2H), 2.40-2.01 (m, 4H) IR: 3315, 2968, 1637, 1543, 1244, 1155, 927, 709 Example 26 4-[(S)-N-[(R)-N'-ethoxycarbonylphenylalanyl] prolyl]aminomethyl-benzamidoxime (compound No. 387 of Table 1) NMR (CDCI3) 7.54 (d, 2H), 7.27-7.19 (m, 7H), 6.31 (d, 1 H), 5.05 (br, 2H), 4.65-4.42 (m, 3H), 4.24-4.10 (m, 1 H), 3.80-3.40 (m, 3H), 3.10-2.95 (m, 2H), 2.60-2.50 (m, 1 H), 2.14 (br, 1 H), 1.95-1.50 (m, 3H), 0.99 (t, 3H) IR: 3339, 1641, 1539, 1451, 1260, 752, 702 ~ ~~:
Example 27 4-[(S)-N-[(R)-2-t-butyloxycarbonylamino-3-cyclohexylpropanoyl]
prolyl]aminomethyl-benzamidoxime (compound No. 397 of Table 1) NMR (CDCI3) 7.75 (br, 1 H), 7.50 (d, 2H), 7.21 (d, 2H), 5.40 (d, 1 H), 4.94 (br, 2H), 4.64 (br, 1 H), 4.40-4.25 (m, 3H), 3.95 (br, 1 H), 3.50-3.40 (m, 1 H), 2.0-0.80 (m, 26H) IR: 3337, 2978, 2924, 2851, 1642, 1536, 1449, 1167 Example 28 4-[(S)-N-[(R)-2-ethoxycarbonylamino-3-methyl-3-methylthiobutanoyl]
prolyl]aminomethyl-benzamidoxime (compound No. 419 of Table 1) NMR (CDCI3) 7.66 (t, 1 H), 7.53 (d, 2H), 7.23 (d, 2H), 5.64 (d, 1 H), 4.91 (s, 2H), 4.68 (d, 1 H), 4.58-4.30 (m, 3H), 3.90 (m, 1 H), 3.87-3.76 (m, 2H), 3.62 (m, 1 H), 2.37 (m, 1 H), 2.09-2.00 (m, 3H), 2.06 (s, 3H), 1.41 (s, 3H), 1.39 (s, 3F1), 1.09 (t, 3H) IR: 3339, 2978, 1641, 1535, 1439, 1249, 1057, 929, 754 Example 29 4-[(S)-N-[(R)-phenyialanyl] prolyl]aminomethyl-benzamidoxime (compound No. 390 of Table 1) dihydrochloride NMR (DMSO-d6) 11.24 (br, 1 H), 9.02 (br, 2H), 8.91 (t, 1 H), 8.80 (br, 3H), 7.66 (d, 2H), 7.44 (d, 2H), 7.35-7.22 (m, 5H), 4.30-4.16 (m, 4H), 3.57-2.95 (m, 3H), 2.45-2.30 (m, 1 H), 1.90-1.20 (m, 4H) IR: 3059, 1649, 1539, 1491, 1454 Example 30 Trans-4-[(S)-N-((R)-2-isopropoxycarbonylamino-2-(:yclohexylacetyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 430 of Table 1) NMR (CDCI3) 7.14 (br, 1 H), 5.70 (d, 1 H), 4.85-4.80 (m, 1 H), 4.70 -4.50 (m, 3H), 4.17-4.08 (m, 2H), 3.96 (br, 1 H), 3.54 (q, 1 H), 3.05 (t, 2H), 2.40-,":'..20 (m, 1 H), 2.09-0.88 (m, 30H) IR: 3342, 2978, 2928, 2855, 1653, 1449, 1256, 1111 Example 31 Trans-4-[(S)-N-((R)-2-t-butoxycarbonylamino-3-cyclohexylpropanoyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 435 of Table 1) NMR (CDCI3) 7.14 (br, 1 H), 5.40 (d, 1 H), 4.60-4.33 (m, 5H), 3.88 (br, 1 H), 3.43 (q, 1 H), 3.20-3.11 (m, 1 H), 3.0-2.96 (m, 1 H), 2.40-2.30 (m, 1 H), 2.0-0.84 (m, 35H) IR: 3356, 2926, 2853, 1649, 1537, 1448, 1167 Example 32 Trans-4-[(S)-N-((R)-2-t-butoxycarbonylamino-2-cyclohexylacetyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 433 of Table 1) NMR (CDCI3) 7.15 (br, 1 H), 5.28 (d, 1 H), 4.58 (br, 4H), 4.09 (t, 1 H), 3.92 (br, 1 H), 3.53 (q, 1 H), 3.20-2.90 (m, 2H), 2.40 (br, 1 H), 2.10-0.91 (m, 33H) IR: 3347, 2930, 2855, 1649, 1541, 1451, 1169 Example 33 Trans-4-[(S)-N-[(R)-2-t-ethoxycarbonylamino-4,4-dirriethylpentanoyl]
prolyl]aminomethylcyclohexanecarboxamidoxime (compourid No. 461 of Table 1) NMR (CDCI3) 7.06 (t, 1 H), 5.56 (d, 1 H), 4.57-4.39 (m, 4H), 4.11 (q, 2H), 3.98 (m, 1 H), 3.47 (m, 1 H), 3.05 (m, 2H), 2.39 (m, 1 H), 2.04-1.78 (m, 10H), 1.57 (d, 2H), 1.56-1.12 (m, 2H), 1.24 (t, 3H), 0.99 (s, 9H), 0.99-0.89 (m, 2H) IR: 3356, 2934, 1649, 1541, 1446, 1249, 1059, 927 Example 34 Trans-4-[(S)-N-[(R)-2-methoxycarbonylamino-4,4-dinnethylpentanoyl]
prolyl]aminomethylcyclohexanecarboxamidoxime (compourid No. 458 of Table 1) <~
NMR (CDCI3) 7.04 (t, 1 H), 5.53 (d, 1 H), 4.68 (s, 2H), 4.56 (d, 1 H), 4.43 (m, 1 H), 3.98 (m, 1 H), 3.66 (s, 3H), 3.47 (m, 1 H), 3.07 (m, 2H), 2.39 (m, 1 H), 2.19-1.77 (m, 8H), 1.57 (d, 2H), 1.55-1.25 (m, 4H), 0.99 (s, 9H), 0.93 (m, 2H) IR: 3344, 2949, 1712, 1649, 1548, 1448, 1249, 1059 Example 35 Trans-4-[(S)-N-[(R)-2-t-butoxycarbonylamino-4,4-dirnethylpentanoyl]
prolyl]aminomethylcyclohexanecarboxamidoxime (compourid No. 467 of Table 1) NMR (CDCI3) 7.12 (t, 1 H), 5.14 (d, 1 H), 4.58 (d, 1 H), 4.53 (s, 2H), 4.37 (m, 1 H), 3.92 (m, 1 H), 3.45 (m, 1 H), 3.19 (m, 1 H), 2.95 (m, 1 H), 2.42 (m, 1 H), 2.06-1.79 (m, 8H), 1.53 (d, 2H), 1.52-1.34 (m, 4H), 1.43 (s, 9H), 0.99 (s, 9H), 1.00-0.89 (m, 2H) IR: 3358, 2930, 1649, 1535, 1448, 1367, 1249, 1168 Example 36 Trans-4-[(S)-N-[(R)-2-benzyloxycarbonylamino-4,4-dimethylpentanoyl]
prolyl]aminomethylcyclohexanecarboxamidoxime (compourid No. 469 of Table 1) NMR (CDCig) 7.36-7.27 (m, 5H), 7.04 (t, 1 H), 5.63 (d, 1 H), 5.16-5.00 (m, 2H), 4.58-4.46 (m, 4H), 3.97 (m, 1 H), 3.47 (m, 1 H), 3.06-2.92 (m, 2H), 2.43-2.38 (m, 1 H), 2.01-1.72 (m, 8H), 1.58 (d, 2H), 1.50-1.23 (m, 4H), 0.98 (s, 9H), 0.98-0.88 (m, 2H) IR: 3356, 2928, 1649, 1541, 1448, 1249, 1053 929 Example 37 Trans-4-[(S)-N-[(R)-2-isopropoxycarbonylamino-4,4-dimethylpentanoyl]
prolyl] aminomethylcyclohexanecarboxamidoxime (compoiund No. 464 of Table 1) NMR (CDCI3) 7.11 (t, 1 H), 5.49 (d, 1 H), 4.83 (m, 1 H), 4.56 (m, 3H), 4.42 (dd, 1 H), 3.98 (m, 1 H), 3.47 (dd, 1 H), 3.04 (m, 2H), 2.40 (m, 1 H), 2.01 (m, 2H), 1.92 (m, 3H), 1.80 (m, 3H), 1.57 (d, 2H), 1.39 (m, 4H), 1.21 (m, 6H), 0.99 (s, 9H), 0.94 (m, 2H) IR: 3343, 1649, 1541, 1449, 1275 Example 38 Trans-4-[(S)-N-[(R)-2-isopropoxycarbonylamino-2-cyclopentylacetyl]
prolyl]aminomethylcyclohexanecarboxamidoxime (compourid No. 464 of Table 1) NMR (CDCI3) 7.14 (t, 1 H), 5.42 (d, 1 H), 4.83 (m, 1 H), 4.60 (d, 1 H), 4.52 (s, 2H), 4.13 (m, 1 H), 3.98 (m, 1 H), 3.56 (m, 1 H), 3.04 (m, 2H), 2.35 (m, 1 H), 2.24 (m, 1 H), 2.10-1.30 (m, 20H), 1.23 (dd, 6H), 1.01-0.93 (m, 2H) IR: 3344, 2934, 1649, 1541, 1448, 1275, 1111, 754 Example 39 Trans-4-[(S)-N-((R)-2-t-butoxycarbonylamino-2-cyclopentylacetyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 432 of Table 1) NMR (CDCI3) 7.16 (t, 1 H), 5.16 (d, 1 H), 4.60 (d, 1 H), 4.51 (s, 2H), 4.14 (t, 1 H), 3.94 (m, 1 H), 3.52 (m, 1 H), 3.01 (m, 2H), 2.38 (m, 1 H), 2.23-1.39 (mõ 21 H), 1.43 (s, 9H), 1.17-0.90 (m, 2H) IR: 3350, 2932, 1649, 1541, 1448, 1367, 1251, 1167, 929 Example 40 Trans-4-[(S)-N-((R)-2-ethoxycarbonylamino-3-cyclohexylpropanoyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 428 of Table 1) NMR (CDCI3) 7.08 (br, 1 H), 5.53 (d, 1 H), 4.80-4.40 (m, 4H), 4.10-3.85 (m, 4H), 3.44 (q, 1 H), 3.06 (t, 3H), 2.15-0.90 (m, 29H) IR: 3343, 2926, 2853, 1649, 1541, 1449, 1260, 1053 Example 41 Trans-4-[(S)-N-((R)-2-isopropoxycarbonylamino-3-cyclohexyl-propanoyl) prolyl] aminomethylcyclohexanecarboxamidoxirne (compound No. 431 of Table 1) NMR (CDCI3) 7.12 (br, 1 H), 5.51 (d, 1 H), 4.85-4.70 (m, 1 H), 4.60-4.30 (m, 4H), 4.0-3.85 (m, 1 H), 3.44 (q, 1 H), 3.10-2.95 (m, 3H), 2.45-2.35 (m, 1 H), 2.05-0.80 (m, 32H) IR: 3347, 2978, 2926, 2853, 1649, 1539, 1449, 1261, 1111 214 059 8 _ Example 42 Trans-4-[(S)-N-((R)-2-isopropoxycarbonylamino-4-ethyl-hexanoyl) prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 463 of Table 1) NMR (CDCI3) 7.11 (t, 1 H), 5.41 (d, 1 H), 4.83 (m, 1 H), 4.56 (m, 3H), 4.39 (m, 1 H), 3.94 (m, 1 H), 3.46 (m, 1 H), 3.02 (m, 2H), 2.39 (m, 1 H), 2.10-1.20 (m, 20H), 1.22 (dd, 6H), 1.02-0.84 (m, 2H), 0.86 (t, 6H) IR: 33346, 2962, 2930, 1653, 1541, 1448, 1271, 1113 Example 43 Trans-4-[(S)-N-((R)-2-t-butoxycarbonylamino-4-ethyl-hexanoyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 466 of Table 1) NMR (CDCI3) 7.19 (t, 1 H), 5.14 (d, 1 H), 4.60 (d, 1 H), 4.50 (s, 2H), 433 (m, 1 H), 3.89 (m, 1 H), 3.43 (m, 1 H), 3.15 (m, 1 H), 2.95 (m, 1 H), 2.40 (m, 1 H), 2.10-1.19 (m, 20H), 1.43 (s, 9H), 1.04-0.89 (m, 2H), 0.86 (t, 6H) IR: 3346, 2964, 2930, 1649, 1541, 1448, 1367, 1280, 1251, 1168, 929 Example 44 Trans-4-[(S)-N-((R)-2-ethoxycarbonylamino-heptanoyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 459 of Table 1) `~.
,,. A. .
NMR (CDCI3) 7.08 (t, 1 H), 5.60 (d, 1 H), 4.58 (m, 3H), 4.35 (m, 1 H), 4.07 (m, 2H), 3.92 (m, 1 H), 3.48 (m, 1 H), 3.06 (m, 2H), 2.40 (m, 1 H), 2.04-1.32 (m, 20H), 1.24 (t, 3H), 0.89 (t, 3H), 0.98 (m, 2H) I R: 3346, 2928, 1649, 1541, 1448, 1255, 1055, 927 Example 45 Trans-4-[(S)-N-((R)-N'-t-butoxycarbonylamino-methionyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 468 of Table 1) NMR (CDCI3) 7.07 (m, 1 H), 5.31 (d, 1 H), 4.55 (m, 4H), 3.56 (m, 1 H), 3.10 (m, 2H), 2.57 (t, 2H), 2.37 (m, 1 H), 2.11 (s, 3H), 2.06-1.29 (m, 14H), 1.43 (s, 9H), 1.00 (m, 2H) IR: 3354, 2928, 1647, 1541, 1448, 1367, 1251, 1167 Example 46 Trans-4-[(S)-N-((R)-2-hydroxy-4,4-dimethyl-pentanoyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 454 of Table 1) NMR (CDCI3) 7.19 (t, 1 H), 4.68 (s, 2H), 4.50 (d, 1 H), 4.36 (t, 1 H), 3.64 (t, 1 H), 3.39 (m, 1 H), 3.06 (m, 2H), 2.35 (m, 2H), 2.16-1.79 (m, 9H), 1.44 (d, 2H), 1.43-1.25 (m, 3H), 1.00-0.95 (m, 2H), 1.02 (s, 9H) IR: 3337, 2944, 1653, 1620, 1566, 1448, 1386, 1248; 1087' '*~.
Example 47 Trans-4-[(S)-N-((R)-2-ethoxycarbonylamino-4-ethyl-hexanoyl) prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 460 of Table 1) NMR (CDCI3) 7.07 (t, 1 H), 5.53 (d, 1 H), 4.56 (m, 3H), 4.40 (m, 1 H), 4.11 (q, 2H), 3.96 (m, 1 H), 3.45 (m, 1 H), 3.05 (m, 2H), 2.36 (m, 1 H), 2.09-1.7"d' (m, 10H), 1.61-1.21 (m, 8H), 1.24 (t, 3H), 1.02-0.83 (m, 2H), 0.86 (t, 6H) IR: 3342, 2962, 2930, 1649, 1541, 1448, 1379, 1269, 1059, 929 Example 48 Trans-4-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl]
prolyl] aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 531 of Table 1) To a solution of the compound (4.2 g, 8.9 mmol) obtained in Example 33 and triethylamine (1.9 ml, 13.3 mmol) in dichloromethane (100 ml), a solution of methyl chloroformate (1.0 g, 10 mmol) in dichloromethane (10 ml) is added at O'C. After stirring for 4 hours, the organic layer is washed once with an aqueous saturated sodium bicarbonate solution, water and saturated brine, successively. After drying over sodium sulfate, the solvent is evaporated and the residue is purified with silica gel column chromatography (ethyl acetate-methanol) to give 2.9 g of the titled compound (62%).
NMR (CDCI3) 0.89-1.07 (m, 11 H), 1.21-1.60 (m, 8H), 1.79-2.40 (m, 9H), 3.0-3.10 (m, 2H), 3.40-3.50 (m, 1 H), 3.84 (s, 3H), 3.84-4.20 (m, 3H), 4.35-4.40 (m, 1 H), 4.55 i`:~
(d, 1 H), 4.81 (br, 2H), 5.19 (d, 1 H), 7.12 (t, 1 H) IR: 3345, 2953, 1763, 1699, 1645, 1541, 1443, 1256 According to the same procedures, the compounds shown in the following Examples were synthesized.
Example 49 4-[(S)-N-((R)-2-hydroxy-2-cyclohexylacetyl) prolyl]arninomethyl-benzamide O-ethoxycarbonyloxime (compound No. 543 of Table 1) NMR (CDCI3) 7.56 (d, 2H), 7.47 (t, 1 H), 7.22 (d, 2H), 5.35 (s, 2H), 4.53 (m, 2H), 4.37 (d, 2H), 4.30 (q, 2H), 4.07 (m, 1 H), 3.64 (m, 1 H), 3.47 (m, 1 H), 3.39 (m, 1 H), 2.35-1.17 (m, 15H), 1.35 (t, 3H) IR: 3368, 2928, 1772, 1628, 1554, 1452, 1404, 1228, 1087, 856 Example 50 Trans-4-[(S)-N-((R)-2-hydroxy-4,4-dimethylpentanoyl) prolyl]
aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 534 of Table 1) NMR (CDCI3) 7.07 (t, 1 H), 4.77 (s, 2H), 4.52 (d, 1 H), 4.34 (m, 1 H), 3.85 (s, 3H), 3.58 (t, 1 H), 3.37 (m, 1 H), 3.22 (d, 1 H), 3.12-3.05 (m, 2H), 2.26-2.21 (m, 1 H), 1.97-1.37 (m, 13H), 1.03 (s, 9H), 1.09-0.95 (m, 2H) IR: 3346, 2953, 1763, 1643, 1442, 1257, 1089, 879 Example 51 Trans-4-[(S)-N-((R)-2-hydroxy-4,4-dimethylpentanoyl)prolyl]
aminomethylcyclohexanecarboxamide O-ethoxycarbonyloxime (compound No. 556 of Table 1) NMR (CDCI3) 7.05 (t, 1 H), 4.73 (s, 2H), 4.52 (d, 1 H), 4.34 (t, 1 H), 4.27 (q, 2H), 3.58 (m, 1 H), 3.45 (m, 1 H), 3.08 (m, 2H), 2.44 (m, 1 H), 2.30-1.30 (m, 13H), 1.32 (t, 3H), 1.03 (s, 9H), 1.07-0.92 (m, 2H) IR: 3373, 2953, 1759, 1641, 1450, 1369, 1248, 1093 Example 52 Trans-4-amino-[(S)-N-[(R)-N'-methanesulfonylphenyPalanyl] prolyl]
aminomethylcyclohexane (compound No. 776 of Table 1) L-tartrate.
(a) Trans-4-t-butyloxycarbonylamino-benzyloxycarbonylamino--methylcyclohexane To a solution of trans-4-aminomethylcyclohexanecarboxylic acid (15.7 g, 100 mmol) and sodium hydroxide (4.0 g, 100 mmol) in water (30 ml), benzyloxycarbonyl chloride (15.6 ml, 110 mmol) and sodiurn hydroxide (4.4 g, 110 mmol) in water (30 ml) are added dropwise at 0 C, simultaneously. After stirring for 4 hours, the mixture is extracted once with ether and 1 N-hydrochloric acid is added to the aqueous layer until the pH of the mixture indicates 2. Then, the precipitated white solid is collected and dried.
To a solution of the resulting compound (12.8 g, 50 nimol) in t-butanol (150 ml), triethylamine (8.3 ml, 60 mmol) and DPPA (13.7 g, 50 mmol) are ~~.
~' .
2f40598 added and heated at reflux for 8 hours. After the solvent is evaporated, water is added to the residue and the mixture is extracted with chloroform. The organic layer is washed once with an aqueous sodium carbonate (5%), once with an aqueous potassium hydrogensulfate (5%), twice with water and once with saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the residue is purified with silica gel column chromatography (hexane-ethyl acetate) to give 8.6 g of the titled compound (47%).
NMR (CDCI3) 0.85-1.37 (m, 14H), 1.60-1.85 (m, 4H), 2.84 (t, 1 H), 3.12 (br, 1 H), 5.00 (s, 2H), 6.62 (d, 1 H), 7.23-7.39 (m, 6H) (b) Trans-4-t-butyloxycarbonylamino-[(S)-N-benzyloxycarbonylprolylJ
aminomethylcyclohexane The compound (4.4 g, 12 mmol) obtained in the item (a) is dissolved in methanol (200 ml) and the catalytic hydrogenation is conducted at room temperature and under atomospheric pressure in the presence of palladium black (0.4 g). After the completion of the reaction, the catalyst is filtered off and the solvent is evaporated.
To a solution of (S)-Z-proline (3.0 g, 12 mmol) in THF (30 ml), CDI (2.0 g, 12 mmol) is added at 0 C. After stirring for 3 hours, a solution of the compound obtained in the above reaction in THF (150 ml) is added at 0 C. After stirring for 6 hours, the solvent is evaporated and water (50 ml) is added to the residue.
The mixture is extracted with chloroform and the organic layer is washed three 2140598 _ times with water and once with saturated brine, successively. After drying over sodium sulfate, the solvent is evaporated and the residue is purified with silica gel chromatography (chloroform-methanol) to give 4.2 g of the titled compound (77%).
NMR (CDCI3) 0.85-1.06 (m, 4H), 1.44 (s, 9H), 1.60-2.35 (m, 9H), 2.94-3.20 (m, 2H), 3.20-3.55 (m, 3H), 4.31 (br, 1 H), 4.47 (br, 1 H), 5.14 (s, 2H), 6.90 (br, 1 H), 7.15-7.40 (m, 5H) (c) Trans-4-t-butyloxycarbonylamino-[(S)-N-[(R)-N'-benzyloxycarbonylphenylalanyl] prolyl] aminomethylcyclohexane The compound (3.6 g, 7.9 mmol) obtained in the item (b) is dissolved in methanol (50 ml) and the catalytic hydrogenation is conducted at room temperature and under atomospheric pressure in the presence of palladium black (0.3 g). After the completion of the reaction, the catalyst is filtered off and the solvent is evaporated.
To a solution of (R)-Z-phenylalanine (2.4 g, 7.9 mmol) in THF (30 ml), CDI (1.3 g, 7.9 mmol) is added at O'C. After stirring for 4 hours, a solution of the compound obtained in the above reaction in THF (60 ml) is added. After stirring for 8 hours, the solvent is evaporated and water is added to the reaction mixture. The mixture is extracted with chloroform and the organic layer is washed three times with water and once with saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the residue is purified with silica gel column chromatography (chloroforrn-methanol) to give J'" '.
4.2 g of the titled compound (89%).
NMR (CDCI3) 0.85-1.06 (m, 5H), 1.33-2.0 (m, 15H), 2.10-2.22 (m, '1 H), 2.50-2.60 (m, 1 H), 2.94-3.01 (m, 5H), 3.30 (br, 1 H), 3.57 (t, 1 H), 4.32-4.59 (m, 3H), 5.08 (d, 2H), 5.69 (d, 1 H), 7.02 (br, 1 H), 7.18-7.37 (m, 10H) (d) Trans-4-amino-[(S)-N-[(R)-N'-methanesulfonylphenylalanyl]prolyl]
aminomethylcyclohexane L-tartrate.
The compound (2.4 g, 3.9 mmol) obtained in the iteni (c) is dissolved in methanol (40 ml) and the catalytic hydrogenation is conducted at room temperature and under atomospheric pressure in the presence of palladium black (0.2 g). After the completion of the reaction, the catalyst is filtered off and the solvent is evaporated. To a solution of the resulting compound in dichloromethane (40 ml), triethylamine (0.65 nnl, 4.7 mmol) is added and a solution of methanesulfonyl chloride (0.47 g, 4.1 mmol) in dichloromethane (100 ml) is further added at 0 C. After stirring for 3 hours, an aqueous saturated sodium bicarbonate solution is added and the organic layer is washed once with water and saturated brine, successively. After drying over sodium sulfate, the solvent is evaporated and the residue is purified with silica gel chromatography (chloroform-methanol).
The resulting compound is dissolved in chloroform (10 ml) and a 4N-dioxane hydrochloride in dioxane (10 ml) is added at 0 C. After stirring for 2 hours, the solvent is evaporated and chloroform (10 ml) and a 1 N-sodium hydroxide solution (10 ml) are added to the residue and, further, the mixture is stirred for 10 minutes. The organic layer is dried over sodium sulfate and a solution of L-tartaric acid (0.34 g, 2.26 nm) in methanol (5 rnl) is added.
The solvent is evaporated and ether (20 ml) is added, and then the precipitated white solid is collected and dried to give 1.36 g of the titled compound (58%).
NMR (DMSO-d6) 7.77 (m, 4H), 7.28 (m, 5H), 4.28 (m, 1 H), 4.16 (m, 1 H), 3.57-3.45 (m, 8H), 2.73 (s, 3H), 1.91-1.75 (m, 9H), 1.54 (m, 1 H), 1.25 (m, 4H), 0.93 (m, 2H) IR: 3324, 2934, 1734, 1638, 1545, 1453, 1308, 1148 According to the same procedures, the compounds shown in the following Examples were synthesized.
Example 53 Trans-4-amino-[(S)-N-[(R)-2-methylsulfonylamino-2-cyclohexylacetyl]
prolyl]aminomethylcyclohexane (compound No. 759 of Table 1) hydrochloride NMR (DMSO-d6) 8.09 (br, 3H), 7.80 (t, 1 H), 7.39 (d, 1 H), 4.30-4.26 (m, 1 H), 3.87 (t, 1 H), 3.80-3.45 (m, 2H), 3.0-2.80 (m, 3H), 2.85 (s, 3H), 2.10-0.80 (m, 24H) IR: 3382, 2930, 2857, 1638, 1543, 1451, 1154 Example 54 Trans-4-amino-[(S)-N-[(S)-N'-benzenesulfonyl-a-glutamyl] prolyl]
aminomethylcyclohexane (compound No. 792 of Table 1) hydrochloride NMR (DMSO-d6) 8.04 (br, 3H), 7.75-7.50 (m, 5H), 4.05 (q, 1 H), 3.77-3.30 (m, 5H), 3.0-2.70 (m, 3H), 2.28 (t, 2H), 2.0-1.52 (m, 10H), 1.31-1.11 (m, 3H), 1.0-0.85 (m, 2H) IR: 3400, 2937, 1637, 1449, 1161 Example 55 Trans-4-amino-[(S)-N-((RS)-3-methylsulfonylamino==3-phenylpropanoyl) prolyl]aminomethylcyclohexane (compound No. 777 of Table 1) hydrochloride NMR (DMSO-d6) 8.08 (m, 3H), 7.34 (m, 5H), 4.78 (m, 1 H), 4.15 (m, 2H), 3.51 (m, 1 H), 3.36 (m, 2H), 2.86 (m, 4H), 2.68 (s, 3H), 2.51 (m, 2H), 2.00-1.69 (m, 6H), 1.27 (m, 4H), 0.92 (m, 2H) IR: 3409, 2936, 1638, 1453, 1314, 1148 Example 56 Trans-4-amino-[(S)-N-((R)-2-isopropoxycarbonylamino-4,4-dimethylpentanoyl) prolyi]aminomethylcyclohexane (compound No. 797 of Table 1) NMR (CDCI3) 7.19 (m, 1 H), 5.32 (d, 1 H), 4.82 (m, 1 H), 4.53 (m, 2H)õ 4.00 (m, 1 H), 3.48 (m, 1 H), 3.03-2.16 (m, 6H), 2.00-1.81 (m, 6H), 1.57 (d, 2H), 1.49 (m, 4H), 1.24 (m, 6H), 1.00 (s, 9H), 0.95 (m, 2H) IR: 3326, 2949, 1640, 1541, 1449, 1248 Example 57 Trans-4-amino-[(S)-N-((R)-N'-ethoxycarbonyl-phenylalanyl) prolyl]
aminomethylcyclohexane (compound No. 780 of Table 1) hydrochloride NMR (DMSO-d6) 7.98 (m, 3H), 7.37 (t, 1 H), 7.26 (m, 5H), 4.37 (dd, 1 H), 4.16 (m, 1 H), 4.02 (m, 2H), 3.88 (m, 1 H), 3.59 (m, 1 H), 3.43 (m, 1 H), 2.86 (m, 5H), 1.93-1.75 (m, 7H), 1.28 (m, 4H), 1.15 (t, 3H), 0.92 (m, 2H) ( R: 3349, 2936, 1642, 1537, 1451, 1258 Example 58 Trans-4-amino-[(S)-((R)-phenylalanyl) prolyl]aminorriethylcyclohexane (compound No. 779 of Table 1) hydrochloride NMR (DMSO-d6) 8.69 (br, 3H), 8.09 (br, 4H), 7.37-7.20 (m, 5H), 4.19 (br, 1 H), 4.09-4.06 (m, 1 H), 3.20-2.82 (m, 5H), 2.0-0.85 (m, 15H) IR: 3426, 2936, 1649, 1539, 1497, 1454 Example 59 Trans-4-amino-[(S)-N-((R)-2-ethoxycarbonyloxy-3-phenylpropanoyl) prolyl]aminomethylcyclohexane (compound No. 785 of Table 1) hydrochloride NMR (DMSO-d6) 7.78 (m, 3H), 7.30 (m, 5H), 7.15 (d, 1 H), 5.22 (t, 1 H), 4.20 (m, 1 H), 4.08 (m, 3H), 3.64 (m, 1 H), 3.02-2.88 (m, 5H), 1.92-1.72 (m, 7H), 1.20-0.94 (m, 9H) IR: 3397, 2938, 1740, 1655, 1453, 1269 Example 60 Trans-4-amino-[(S)-N-((R)-2-allylcarbamoyloxy-3-phenylpropanoyl) prolyl]aminomethylcyclohexane (compound No. 787 of Table 1) hydrobromide NMR (DMSO-d6) 7.90 (m, 3H), 7.30 (m, 5H), 7.14 (m, 1 H), 5.72 (m, 2HI), 5.06 (m, 2H), 4.76 (m, 1 H), 4.17 (m, 1 H), 3.60 (m, 1 H), 2.98-2.85 (m, 5H), 1.87-1.70 (m, 7H), 1.23 (m, 7H), 0.90 (m, 2H) IR: 3364, 2936, 1707, 1645, 1543, 1454, 1256 Example 61 Trans-4-amino-[(S)-N-((R)-2-hydroxy-2-cyclohexylacetyl) prolyl]
aminomethylcyclohexane (compound No. 768 of Table 1) hydrochloride NMR (DMSO-d6) 8.21 (br, 3H), 7.95 (m, 1 H), 4.53 (m, 1 H), 4.18 (d, 1 H), 3.95 (m, 1 H), 3.07 (m, 3H), 2.18-1.55 (m, 22H), 1.30-1.03 (m, 2H) IR: 3422, 2928, 2854, 1637, 1450, 1388, 1240, 1114, 1045 Example 62 Trans-4-amino-[(S)-N-((R)-2-hydroxy-2-phenylacetyl) prolyl]
aminomethylcyclohexane (compound No. 783 of Table 1) hydrochloride :~.
NMR (DMSO-ds) 2 14059 8 7.98 (br, 3H), 7.37-7.28 (m, 5H), 5.48 (br, 1 H), 5.23 (id, 1 H), 4.23 (d, 1 H), 3.70-3.35 (m, 2H), 3.0-2.80 (m, 4H), 2.0-1.60 (m, 8H), 1.40-0.90 (m, 5H) IR: 3329, 2935, 1667, 1626, 1552, 1448 Example 63 Trans-4-amino-[(RS)-1-((R)-N'-methylsulfonyi-phenylalanyl)-2-piperidinecarboxyl]aminomethylcyclohexane (compound No. 834 of Table 1) hydrochloride NMR (DMSO-d6) 8.07 (m, 3H), 7.28 (m, 5H), 4.64 (m, 1 H), 4.39 (m, 1 H), 3.99 (m, 1 H), 3.67 (m, 1 H), 2.87 (m, 7H), 2.84 (s, 3H), 1.91-1.68 (m, 5H), 1.33-0.92 (m, 10H) IR: 3385, 2936, 1638, 1535, 1453, 1314, 1150 Example 64 Trans-4-amino-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl] prolyl]aminomethylcyclohexane (compound No. 794 of Table 1) NMR (CDCI3) 7.16 (m, 1 H), 5.68 (d, 1 H), 4.53 (d, 1 H), 4.38 (m, 1 H), 4.10 (q, 2H), 4.01 (m, 1 H), 3.46-3.07 (m, 4H), 2.30-1.81 (m, 8H), 1.58 (m, 5H), 1.26 (t, 3H), 1.00 (s, 9H), 0.95 (m, 2H) I R: 3329, 2949, 1642, 1541, 1447, 1248, 1059 ,rw Example 65 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl] prolyl]aminornethylcyclohexane (compound No. 968 of Table 1) To a solution of the compound (5.4 g, 11.7 mmol) obtained in Example 64 in DMF (40 ml), sodium carbonate (3.2 g, 23.4 mmol) is added, and a solution of 4-bromomethyl-5-methyl-1,3-dioxo-2-on (4.0 g, 17.6 mmol) in DMF
(5 ml) is further added at 0 C. After stirring for 48 hours, the solvent is evaporated and water is added to the residue, which is extracted with ethyl acetate. The organic layer is washed three times with water and once with saturated brine, successively, and then dried over sodium sulfate. The solvent is evaporated and the residue is purified with silica gel column chromatography (chloroform-methanol) to give 2.8 g of the titled compound (44%).
NMR (CDCI3) 7.07 (m, 1 H), 5.15 (d, 1 H), 4.56 (d, 1 H), 4.41 (m, 1 H), 4.10 (q, 2H), 4.00 (m, 2H), 3.48 (s, 2H), 3.45 (m, 2H), 3.04 (t, 1 H), 2.62 (m, 1 H), 2.38 (m, 1 H), 2.11 (s, 3H), 2.00 (m, 3H), 1.82 (m, 2H), 1.73-1.43 (m, 4H), 1.28 (1:, 3H), 1.26 (m, 3H), 1.00 (s, 9H), 0.96 (m, 2H) IR: 3329, 2934, 2870, 1823, 1649, 1539, 1445, 1223 According to the same procedures, the compounds shown in the following Examples were synthesized.
Example 66 Trans-4-t-butoxycarbonylamino-[(S)-N-[(R)-N'-methanesulfonyl-~, ~~..~
~~ ';~I~
2140598 .
phenylalanyl] prolyl]aminomethylcyclohexane (compound No. 955 of Table 1) NMR (CDCI3) 7.29 (m, 3H), 7.24 (m, 2H), 6.67 (t, 1 H), 5.61 (d, 1 H), 4.40 (m, 2H), 4.29 (dd, 1 H), 3.58 (m, 1 H), 3.34 (m, 1 H), 2.99 (m, 4H), 2.82 (s, 3H), 2.69 (m, 1 H), 2.18-1.74 (m, 9H), 1.43 (s, 9H), 1.02 (m, 4H) IR: 3376, 2932, 1655, 1526, 1453, 1322 Example 67 Trans-4-guanidino-[(S)-N-[(R)-N'-methanesulfonylphenylalanyl) prolyl]aminomethylcyclohexane (compound No. 646 of Table 1) sulfate To a solution of the compound (0.45 g, 1 mmol) obtained in Example 52 in ethanol (15 mi), a solution of 2-methylisothiourea sulfate (0.14 g, 0.5 mmol) in water (5 ml) is added and heated at reflux for 6 hours. Ttie solvent is evaporated and ether (20 ml) is added. The precipitated white solid is collected and washed with ether, and then dried under reduced pressure to give 0.44 g of the titled compound (81 %).
NMR (DMSO-d6) 8.04-2.0 (m, 13H), 2.60-3.96 (m, 7H), 2.77 (s, 3H), 4.14-4.28 (m, 2H), 5.47 (br, 1 H), 6.75 (br, 1 H), 7.20-7.36 (m, 5H), 7.83 (br, 1 H), 8.40 (br, 4H) IR: 3322, 2932, 2193, 2153, 1644, 1545, 1451, 1319, 1150 According to the same procedure as that described iri Example 1, the following compounds of Examples 68 to 78 were synthesized.
Example 68 4-Amidino-[(S)-N-[(R)-2-hydroxy-cyclohexylacetyl] prolyl]
aminomethylbenzene (compound No. 82 of Table 1) hydrochloride NMR (DMSO-d6) 9.29 (br, 2H), 8.93 (br, 2H), 8.51 (t, 1 H), 7.75 (d, 2H), 7.49 (d, 2H), 4.37 (m, 3H), 3.96 (d, 1 H), 3.70 (m, 1 H), 3.60-3.40 (m, 2H) 2.20-1.0 (m, 14H) IR: 3227, 2922, 1657, 1607, 1539, 1485, 1458, 1323, 1246, 1032 Example 69 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-3,3-dimethylbutanoyl]
prolyl]aminomethylbenzene (compound No. 114 of Table 1) hydrochloride NMR (DMSO-d6) 9.41 (br, 2H), 9.24 (br, 2H), 8.63 (t, 1 H), 7.81 (d, 2H), 7.47 (d, 2H), 7.20 (d, 1 H), 4.42 (dd, 1 H), 4.35 (t, 2H), 3.96 (d, 1 H), 3.80-3.60 (m, 2H), 2.85 (s, 3H), 2.20-1.80 (m, 4H), 0.97 (s, 9H) IR: 3273, 2970, 2365, 1630, 1541, 1483, 1412, 1304, 1153, 715 Example 70 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-6-ethoxycarbonyl-hexanoyl] prolyl]aminomethylbenzene (compound No. 117 of Table 1) hydrochloride NMR (DMSO-d6) 9.35 (br, 4H), 8.66 (t, 1 H), 7.79 (d, 1 H), 7.48 (d, 2H), 4.35 (m, 3H), 4.65 (q, 2H), 3.69 (m, 1 H), 3.55 (m, 1 H), 2.75 (s, 3H), 2.29 (t, 2H), 2.13 (m, 2H), 1.94 (m, 2H), 1.85 (m, 2H), 1.52 (m, 7H), 1.18 (t, 3H) IR: 3382, 1644, 1547, 1427, 1375, 1314, 1150, 1111 Example 71 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-4-(3'-carboxy)-phenyl-butanoyl] prolyl]aminomethylbenzene (compound No. 119 of Table 1) hydrochloride NMR (DMSO-d6) 9.45 (s, 2H), 9.38 (s, 2H), 8.62 (t, 1 H), 7.84 (m, 2H), 7.79 (d, 2H), 7.64 (d, 1 H), 7.47 (d, 2H), 7.42 (m, 2H), 4.33 (m, 3H), 4.10 (m, 1 H), 3.57-3.37 (m, 2H), 2.85 (m, 1 H), 2.78 (s, 3H), 2.73 (m, 1 H), 2.12 (m, 1 H), 1.95-1.81 (m, 6H) IR: 3366, 1638, 1543, 1489, 1449, 1311, 1150, 754, 527 Example 72 4-Amidino-[(S)-N-[(R)-N'-methylsulfonyl-O-(4'-carboxyphenyl)-seryl]
prolyl]aminomethylbenzene (compound No. 970 of Table 1) hydrochloride NMR (DMSO-d6) 9.31 (s, 2H), 9.00 (s, 2H), 8.59 (t, 1 H), 7.90 (d, 2H), 7.83 (d, 1 H), 7.75 (d, 2H), 7.48 (d, 2H), 7.03 (d, 2H), 4.35 (m, 4H), 4.22 (m, 2H), 4.12 (dd, 1 H), 3.72 (m, 2H), 2.89 (s, 3H), 2.20-1.80 (m, 4H) IR: 3376, 1647, 1607, 1424, 1318, 1252, 1154, 1119, 774, 633, 525 Example 73 4-Amidino-[(S)-N-[(R)-N'-methylsulfonyl-O-ethoxycarbonylmethyl-tyrosyl]
prolyl]aminomethylbenzene (compound No. 971 of Table 1) hydrochloride NMR (DMSO-d6) 9.41 (br, 2H), 9.20 (br, 2H), 8.56 (t, 1 H), 7.80 (d, 2H), 7.65 (d, 1 H), 7.48 (d, 2H), 7.18 (dd, 2H), 6.84 (dd, 2H), 4.75 (q, 1 H), 4.30 (ddõ 1 H), 4.30-4.25 (m, 2H), 3.70-3,.42 (m, 3H), 3.47 (q, 2H), 3.18 (t, 1 H), 2.83 (d, 2H), 2.72 (s, 3H), 1.89-1.60 (m, 4H), 1.14 (dt, 3H) IR: 3370, 2365, 1742, 1636, 1541, 1512, 1445, 1308 Example 74 4-Amidino-[(S)-N-[(R)-N'-ethoxycarbonylphenylalanyl] prolyl]
aminomethylbenzene (compound No. 972 of Table 1) hydrochloride NMR (DMSO-d6) 9.40 (br, 2H), 9.24 (br, 2H), 8.14 (t, 1 H), 7.80 (d, 2H), 7.59 (t, 1 H), 7.45 (d, 2H), 7.31-7.15 (m, 5H), 4.50-4.26 (m, 4H), 3.90-3.57 (m, 3H), 3.0-2.7 (m, 3H), 1.9-1.6 (m, 4H), 1.10-1.0 (m, 3H) IR: 3279, 2364, 1637, 1539, 1491, 1450, 1255, 704 Example 75 4-Amidino-[(S)-N-[(R)-2-methylsulfonylaminoheptanoyl] prolyl]
aminomethylbenzene (compound No. 973 of Table 1) hydrochloride NMR (DMSO-d6) 9.37 (s, 2H), 9.16 (s, 2H), 8.60 (t, 1 H), 7.76 (d, 2H), 7.48 (d, 2H), 7.40 (d, 1 H), 4.50-4.23 (m, 3H), 4.08 (m, 1 H), 3.69 (m, 1 H), 3.36 (m, 1 H), 2.74 (s, 3H), 2.15 (m, 1 H), 2.09-1.84 (m, 3H), 1.61-1.22 (m, 8H), 0.87 (m, 3H) IR: 3366, 2957, 1638, 1543, 1489, 1426, 1314, 1154, 718, 527 Example 76 4-Amidino-[(S)-N-[(R)-N'-methylsulfonyl-O-(3'-carboxymethyl-phenyl)-seryl] prolyl]aminomethylbenzene (compound No. 974 of Table 1) hydrochloride NMR (DMSO-d6) 9.46 (s, 2H), 9.31 (s, 2H), 8.70 (t, 1 H), 7.83 (m, 3H), 7.48 (d, 2H), 7.19 (m, 2H), 6.89 (d, 2H), 4.58 (dd, 1 H), 4.37 (m, 4H), 4.14 (d, 2H), 3.70 (m, 1 H), 3.60 (m, 3H), 2.89 (s, 3H), 2.11 (m, 1 H), 2.01-1.82 (m, 3H) IR: 3382, 1724, 1640, 1543, 1489, 1447, 1316, 1262, 1154, 768, 527 Example 77 4-Amidino-[(S)-N-[(R)-N'-methylsulfonyl-O-(4'-carboxymethyl-phenyl)-seryl] prolyl]aminomethylbenzene (compound No. 975 of Table 1) hydrochloride NMR (DMSO-d6) 9.45 (s, 2H), 9.29 (s, 2H), 8.70 (t, 1H), 7.83 (d, 2H), 7.82 (d, 2H), 7.48 (d, 2H), 7.24 (d, 1 H), 6.82 (d, 2H), 4.59 (dd, 1 H), 4.37 (m, 4H), 4.14 (d, 2H), 3.70 (m, 1 H), 3.61 (m, 3H), 2.89 (s, 3H), 2.11 (m, 1 H), 2.01-1.82 (rn, 3H) IR: 3383, 1640, 1545, 1514, 1437, 1312, 1242, 1152, 824, 523 Example 78 4-Amidino-[(S)-N-[(R)-2-ethoxycarbonylmethylsulfonylamino-heptanoyl]
aminomethylbenzene (compound No. 82 of Table 1) hydrochloride NMR (DMSO-d6) 9.29 (br, 2H), 8.93 (br, 2H), 8.51 (t, 1 H), 7.75 (d, 2H), 7.49 (d, 2H), 4.37 (m, 3H), 3.96 (d, 1 H), 3.70 (m, 1 H), 3.60-3.40 (m, 2H) 2.20-1.0 (m, 14H) IR: 3227, 2922, 1657, 1607, 1539, 1485, 1458, 1323, 1246, 1032 Example 69 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-3,3-dimethylbutanoyl]
prolyl]aminomethylbenzene (compound No. 114 of Table 1) hydrochloride NMR (DMSO-d6) 9.41 (br, 2H), 9.24 (br, 2H), 8.63 (t, 1 H), 7.81 (d, 2H), 7.47 (d, 2H), 7.20 (d, 1 H), 4.42 (dd, 1 H), 4.35 (t, 2H), 3.96 (d, 1 H), 3.80-3.60 (m, 2H), 2.85 (s, 3H), 2.20-1.80 (m, 4H), 0.97 (s, 9H) IR: 3273, 2970, 2365, 1630, 1541, 1483, 1412, 1304, 1153, 715 Example 70 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-6-ethoxycarbonyl-hexanoyl] prolyl]aminomethylbenzene (compound No. 117 of Table 1) hydrochloride NMR (DMSO-d6) 9.35 (br, 4H), 8.66 (t, 1 H), 7.79 (d, 1 H), 7.48 (d, 2H), 4.35 (m, 3H), 4.65 (q, 2H), 3.69 (m, 1 H), 3.55 (m, 1 H), 2.75 (s, 3H), 2.29 (t, 2H), 2.13 (m, 2H), 1.94 (m, 2H), 1.85 (m, 2H), 1.52 (m, 7H), 1.18 (t, 3H) IR: 3382, 1644, 1547, 1427, 1375, 1314, 1150, 1111 Example 71 4-Amidino-[(S)-N-[(R)-2-methylsulfonylamino-4-(3'-carboxy)-phenyl-butanoyl] prolyl]aminomethylbenzene (compound No. 119 of Table 1) hydrochloride NMR (DMSO-d6) 9.45 (s, 2H), 9.38 (s, 2H), 8.62 (t, 1 H), 7.84 (m, 2H), 7.79 (d, 2H), 7.64 (d, 1 H), 7.47 (d, 2H), 7.42 (m, 2H), 4.33 (m, 3H), 4.10 (m, 1 H), 3.57-3.37 (m, 2H), 2.85 (m, 1 H), 2.78 (s, 3H), 2.73 (m, 1 H), 2.12 (m, 1 H), 1.95-1.81 (m, 6H) IR: 3366, 1638, 1543, 1489, 1449, 1311, 1150, 754, 527 Example 72 4-Amidino-[(S)-N-[(R)-N'-methylsulfonyl-O-(4'-carboxyphenyl)-seryl]
prolyl]aminomethylbenzene (compound No. 970 of Table 1) hydrochloride NMR (DMSO-d6) 9.31 (s, 2H), 9.00 (s, 2H), 8.59 (t, 1 H), 7.90 (d, 2H), 7.83 (d, 1 H), 7.75 (d, 2H), 7.48 (d, 2H), 7.03 (d, 2H), 4.35 (m, 4H), 4.22 (m, 2H), 4.12 (dd, 1 H), 3.72 (m, 2H), 2.89 (s, 3H), 2.20-1.80 (m, 4H) IR: 3376, 1647, 1607, 1424, 1318, 1252, 1154, 1119, 774, 633, 525 Example 73 4-Amidino-[(S)-N-[(R)-N'-methylsulfonyl-O-ethoxycarbonylmethyl-tyrosyl]
prolyl]aminomethylbenzene (compound No. 971 of Table 1) hydrochloride NMR (DMSO-d6) 9.41 (br, 2H), 9.20 (br, 2H), 8.56 (t, 1 H), 7.80 (d, 2H), 7.65 (d, 1 H), 7.48 (d, 2H), 7.18 (dd, 2H), 6.84 (dd, 2H), 4.75 (q, 1 H), 4.30 (ddõ 1 H), 4.30-4.25 (m, 2H), 3.70-3,.42 (m, 3H), 3.47 (q, 2H), 3.18 (t, 1 H), 2.83 (d, 2H), 2.72 (s, 3H), 1.89-1.60 (m, 4H), 1.14 (dt, 3H) IR: 3370, 2365, 1742, 1636, 1541, 1512, 1445, 1308 Example 74 4-Amidino-[(S)-N-[(R)-N'-ethoxycarbonylphenylalanyl] prolyl]
aminomethylbenzene (compound No. 972 of Table 1) hydrochloride NMR (DMSO-d6) 9.40 (br, 2H), 9.24 (br, 2H), 8.14 (t, 1 H), 7.80 (d, 2H), 7.59 (t, 1 H), 7.45 (d, 2H), 7.31-7.15 (m, 5H), 4.50-4.26 (m, 4H), 3.90-3.57 (m, 3H), 3.0-2.7 (m, 3H), 1.9-1.6 (m, 4H), 1.10-1.0 (m, 3H) IR: 3279, 2364, 1637, 1539, 1491, 1450, 1255, 704 Example 75 4-Amidino-[(S)-N-[(R)-2-methylsulfonylaminoheptanoyl] prolyl]
aminomethylbenzene (compound No. 973 of Table 1) hydrochloride NMR (DMSO-d6) 9.37 (s, 2H), 9.16 (s, 2H), 8.60 (t, 1 H), 7.76 (d, 2H), 7.48 (d, 2H), 7.40 (d, 1 H), 4.50-4.23 (m, 3H), 4.08 (m, 1 H), 3.69 (m, 1 H), 3.36 (m, 1 H), 2.74 (s, 3H), 2.15 (m, 1 H), 2.09-1.84 (m, 3H), 1.61-1.22 (m, 8H), 0.87 (m, 3H) IR: 3366, 2957, 1638, 1543, 1489, 1426, 1314, 1154, 718, 527 Example 76 4-Amidino-[(S)-N-[(R)-N'-methylsulfonyl-O-(3'-carboxymethyl-phenyl)-seryl] prolyl]aminomethylbenzene (compound No. 974 of Table 1) hydrochloride NMR (DMSO-d6) 9.46 (s, 2H), 9.31 (s, 2H), 8.70 (t, 1 H), 7.83 (m, 3H), 7.48 (d, 2H), 7.19 (m, 2H), 6.89 (d, 2H), 4.58 (dd, 1 H), 4.37 (m, 4H), 4.14 (d, 2H), 3.70 (m, 1 H), 3.60 (m, 3H), 2.89 (s, 3H), 2.11 (m, 1 H), 2.01-1.82 (m, 3H) IR: 3382, 1724, 1640, 1543, 1489, 1447, 1316, 1262, 1154, 768, 527 Example 77 4-Amidino-[(S)-N-[(R)-N'-methylsulfonyl-O-(4'-carboxymethyl-phenyl)-seryl] prolyl]aminomethylbenzene (compound No. 975 of Table 1) hydrochloride NMR (DMSO-d6) 9.45 (s, 2H), 9.29 (s, 2H), 8.70 (t, 1H), 7.83 (d, 2H), 7.82 (d, 2H), 7.48 (d, 2H), 7.24 (d, 1 H), 6.82 (d, 2H), 4.59 (dd, 1 H), 4.37 (m, 4H), 4.14 (d, 2H), 3.70 (m, 1 H), 3.61 (m, 3H), 2.89 (s, 3H), 2.11 (m, 1 H), 2.01-1.82 (rn, 3H) IR: 3383, 1640, 1545, 1514, 1437, 1312, 1242, 1152, 824, 523 Example 78 4-Amidino-[(S)-N-[(R)-2-ethoxycarbonylmethylsulfonylamino-heptanoyl]
prolyl]aminomethylbenzene (compound No. 976 of Table 1) hydrochloride NMR (DMSO-d6) 9.36 (s, 2H), 9.15 (s, 2H), 8.49 (t, 1 H), 7.81 (d, 1 H), 7.77 (d, 2H), 7.47 (d, 2H), 4.35 (m, 3H), 4.21 (d, 1 H), 4.15 (m, 1 H), 4.06 (q, 2H), 3.93 (d, 1 H), 3.73 (m, 1 H), 3.53 (m, 1 H), 2.14 (m, 1 H), 1.94 (m, 3H), 1.67-1.18 (m, 8H), 1.14 (t, 3H), 0.89 (m, 3H) IR: 3274, 2957, 2872, 1821, 1738, 1647, 1541, 1422, 1319, 1159, 1022, 723, 628, 527 According to the same procedures as that described in Example 15, the following compounds of Examples 79 to 86 were synthesized.
Example 79 Trans-4-amidino-[(S)-N-[(R)-N'-ethoxycarbonyl-O-t-butyloxy-seryl]prolyl]
aminomethylcyclohexane (compound No. 240 of Table 1) hydrochloride NMR (DMSO-d6) 8.88 (br, 2H), 8.71 (br, 2H), 7.72 (m, 1 H), 6.39 (m, 1 H), 4.59 (m, 1 H), 4.52 (m, 1 H), 4.11 (m, 2H), 3.86-3.71 (m, 2H), 3.58 (m, 2H), 3.22 (m, 2H), 2.79-0.88 (m, 15H), 1.24 (t, 3H), 1.15 (s, 9H) I R: 3271, 2976, 1685, 1647, 1541, 1448, 1257, 1192, 1095õ 1055 Example 80 Trans-4-amidino-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-(1',1'-dimethylpropyl)-seryl] prolyl]aminomethylcyclohexane (compound No. 977 of Table 1) hydrochloride NMR (DMSO-d6) 8.74 (br, 4H), 7.68 (m, 1 H), 6.01 (m, 1 H), 4.83 (m, 1 H), 4.57 (m, 2H), 3.74 (m, 2H), 3.50 (m, 2H), 3.14 (m, 1 H), 2.97 (m, 1 H), 2.5-0.9 (ni, 16H), 1.24 (dd, 6H), 1.09 (s, 6H), 0.81 (t, 3H) IR: 3314, 2978, 1693, 1641, 1543, 1450, 1375, 1261, 1111, 1059 Example 81 Trans-4-amidino-[(S)-N-[(R)-N'-ethoxycarbonyl-O-(1 ",1'-dimethylpropyl)-seryl] prolyl]aminomethylcyclohexane (compound No. 978 of Table 1) hydrochloride NMR (DMSO-d6) 8.75 (br, 4H), 7.55 (m, 1 H), 6.40 (m, 1 H), 4.52 (m, 2H), 4.13 (m, 2H), 3.88-3.70 (m, 2H), 3.55 (m, 2H), 3.28 (m, 1 H), 2.87-2.70 (m, 1 H), 2.20-1.20 (m, 14H), 1.27 (t, 3H), 1.09 (s, 6H), 0.81 (t, 3H), 1.10-0.90 (m, 21-1) IR: 3292, 2974, 1689, 1645, 1543, 1448, 1259, 1095, 1055 Example 82 Trans-4-amidino-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-(1'-ethyl-1'-methyl-propy!)-seryl] prolyl]aminomethylcyclohexane (compound No. 979 of Table 1) hydrochloride NMR (DMSO-d6) 8.78 (s, 2H), 8.69 (s, 2H), 7.55 (br, 1 H), 5.99 (br, 1 H), 4.84 (m, 1 H), 4.54 (m, 2H), 3.71 (m, 2H), 3.49 (m, 2H), 3.20-0.90 (m, 16H), 1.64 (q, 4H), 1.23 (t, 6H), 1.03 (s, 3H), 0.78 (t, 6H) IR: 3315, 2976, 2934, 1685, 1641, 1543, 1450, 1375, 1261, 1111 Example 83 Trans-4-amidino-[(S)-N-[(R)-N'-ethoxycarbonyl-S-t-butyl-cystinyl]prolyl]
aminomethylcyclohexane (compound No. 980 of Table 1) hydrochloride NMR (DMSO-d6) 8.82 (br, 2H), 8.74 (br, 2H), 7.47 (m, 1 H), 6.63 (m, 1 H), 4.60-4.40 (m, 2H), 4.20-4.21 (m, 2H), 4.00 (m, 1 H), 3.72 (m, 1 H), 3.24 (m, 1 H), 2.87 (m, 2H), 2.65 (m, 1 H), 2.18-1.31 (m, 12H), 1.31 (s, 9H), 1.27 (t, 3H), 1.10-0.90 (m, 2H) IR: 3298, 2932, 1693, 1641, 1541, 1448, 1304, 1257, 1161, 1047 Example 84 Trans-4-amidino-[(S)-N-[(R)-N'-isopropoxycarbonyl-0-(1'-methylcyclopentyl)-seryl] prolyl]aminomethylcyclohexane (compound No. 981 of Table 1) hydrochloride NMR (DMSO-d6) 8.79 (br, 4H), 7.64 (m, 1 H), 5.97 (m, 1 H), 4.83 (m, 1 H), 4.55 (m, 2H), 3.76 (m, 2H), 3.52 (m, 2H), 3.15-1.20 (m, 22H), 1.27-1.13 (m, 9H), 1.13-0.95 (m, 2H) IR: 3329, 2934, 1684, 1639, 1541, 1450, 1261, 1182, 1111, 1060, 918 Example 85 Trans-4-amidino-[(S)-N-[(R)-N'-isopropoxycarbonyl-0-t-butyl-threonyl]
Example 79 Trans-4-amidino-[(S)-N-[(R)-N'-ethoxycarbonyl-O-t-butyloxy-seryl]prolyl]
aminomethylcyclohexane (compound No. 240 of Table 1) hydrochloride NMR (DMSO-d6) 8.88 (br, 2H), 8.71 (br, 2H), 7.72 (m, 1 H), 6.39 (m, 1 H), 4.59 (m, 1 H), 4.52 (m, 1 H), 4.11 (m, 2H), 3.86-3.71 (m, 2H), 3.58 (m, 2H), 3.22 (m, 2H), 2.79-0.88 (m, 15H), 1.24 (t, 3H), 1.15 (s, 9H) I R: 3271, 2976, 1685, 1647, 1541, 1448, 1257, 1192, 1095õ 1055 Example 80 Trans-4-amidino-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-(1',1'-dimethylpropyl)-seryl] prolyl]aminomethylcyclohexane (compound No. 977 of Table 1) hydrochloride NMR (DMSO-d6) 8.74 (br, 4H), 7.68 (m, 1 H), 6.01 (m, 1 H), 4.83 (m, 1 H), 4.57 (m, 2H), 3.74 (m, 2H), 3.50 (m, 2H), 3.14 (m, 1 H), 2.97 (m, 1 H), 2.5-0.9 (ni, 16H), 1.24 (dd, 6H), 1.09 (s, 6H), 0.81 (t, 3H) IR: 3314, 2978, 1693, 1641, 1543, 1450, 1375, 1261, 1111, 1059 Example 81 Trans-4-amidino-[(S)-N-[(R)-N'-ethoxycarbonyl-O-(1 ",1'-dimethylpropyl)-seryl] prolyl]aminomethylcyclohexane (compound No. 978 of Table 1) hydrochloride NMR (DMSO-d6) 8.75 (br, 4H), 7.55 (m, 1 H), 6.40 (m, 1 H), 4.52 (m, 2H), 4.13 (m, 2H), 3.88-3.70 (m, 2H), 3.55 (m, 2H), 3.28 (m, 1 H), 2.87-2.70 (m, 1 H), 2.20-1.20 (m, 14H), 1.27 (t, 3H), 1.09 (s, 6H), 0.81 (t, 3H), 1.10-0.90 (m, 21-1) IR: 3292, 2974, 1689, 1645, 1543, 1448, 1259, 1095, 1055 Example 82 Trans-4-amidino-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-(1'-ethyl-1'-methyl-propy!)-seryl] prolyl]aminomethylcyclohexane (compound No. 979 of Table 1) hydrochloride NMR (DMSO-d6) 8.78 (s, 2H), 8.69 (s, 2H), 7.55 (br, 1 H), 5.99 (br, 1 H), 4.84 (m, 1 H), 4.54 (m, 2H), 3.71 (m, 2H), 3.49 (m, 2H), 3.20-0.90 (m, 16H), 1.64 (q, 4H), 1.23 (t, 6H), 1.03 (s, 3H), 0.78 (t, 6H) IR: 3315, 2976, 2934, 1685, 1641, 1543, 1450, 1375, 1261, 1111 Example 83 Trans-4-amidino-[(S)-N-[(R)-N'-ethoxycarbonyl-S-t-butyl-cystinyl]prolyl]
aminomethylcyclohexane (compound No. 980 of Table 1) hydrochloride NMR (DMSO-d6) 8.82 (br, 2H), 8.74 (br, 2H), 7.47 (m, 1 H), 6.63 (m, 1 H), 4.60-4.40 (m, 2H), 4.20-4.21 (m, 2H), 4.00 (m, 1 H), 3.72 (m, 1 H), 3.24 (m, 1 H), 2.87 (m, 2H), 2.65 (m, 1 H), 2.18-1.31 (m, 12H), 1.31 (s, 9H), 1.27 (t, 3H), 1.10-0.90 (m, 2H) IR: 3298, 2932, 1693, 1641, 1541, 1448, 1304, 1257, 1161, 1047 Example 84 Trans-4-amidino-[(S)-N-[(R)-N'-isopropoxycarbonyl-0-(1'-methylcyclopentyl)-seryl] prolyl]aminomethylcyclohexane (compound No. 981 of Table 1) hydrochloride NMR (DMSO-d6) 8.79 (br, 4H), 7.64 (m, 1 H), 5.97 (m, 1 H), 4.83 (m, 1 H), 4.55 (m, 2H), 3.76 (m, 2H), 3.52 (m, 2H), 3.15-1.20 (m, 22H), 1.27-1.13 (m, 9H), 1.13-0.95 (m, 2H) IR: 3329, 2934, 1684, 1639, 1541, 1450, 1261, 1182, 1111, 1060, 918 Example 85 Trans-4-amidino-[(S)-N-[(R)-N'-isopropoxycarbonyl-0-t-butyl-threonyl]
prolyl]aminomethylcyclohexane (compound No. 982 of Table 1) hydrochloride NMR (DMSO-d6) 8.74 (m, 4H), 7.80 (m, 1 H), 5.66 (m, 1 H), 4.85 (m, 1 H), 4.57 (m, 1 H), 4.29 (m, 1 H), 3.80-3.60 (m, 3H), 3.05 (m, 2H), 2.60 (m, 1 H), 2.50-1.20 (m, 11 H), 1.27-1.22 (m, 15H), 1.15 (d, 3H), 1.10-0.90 (m, 2H) IR: 3331, 2978, 1697, 1639, 1543, 1450, 1375, 1265, 1182, 1111 Example 86 Trans-4-amidino-[(S)-N-[(R)-2-ethoxycarbonylamino.-3-isopropylthio-3-methyl-butanoyl] prolyl]aminomethylcyclohexane (compound No. 983 of Table 1) hydrochloride NMR (DMSO-d6) 9.13 (br, 2H), 8.46 (br, 2H), 7.30 (m, 1 H), 5.85 (m, 1 H), 4.55 (m, 1 H), 4.36 (m, 1 H), 4.15-3.85 (m, 3H), 3.69 (m, 1 H), 3.02 (m, 2H), 2.30 (m, 1 H), 2.00-1.20 (m, 13H), 1.48 (s, 3H), 1.33 (s, 3H), 1.30-1.20 (m, 9H), 1.05-0.85 (m, 2H) IR: 3420, 2974, 1635, 1556, 1521, 1448, 1385, 1298, 1259, 1060 According to the same procedures as that described in Example 24, the following compounds of Examples 87 to 113were synthesized.
Example 87 4-[(S)-N-[(R)-2-hydroxy-cyclohexylacetyl] prolyl]
aminomethylbenzamidoxime (compound No. 391 of Table 1) NMR (DMSO-d6) 9.55 (br, 1 H), 8.31 (t, 1 H), 7.59 (d, 2H), 7.24 (d, 2H), 5.73 (br, 2H), 4.57 (m, 1 H), 4.26-4.32 (m, 3H), 3.91 (br, 1 H), 3.40-3.60 (m, 2H), 2.05-0.80 (m, 15H) IR: 3375, 2926, 2853, 1638, 1561, 1451, 1385, 1244 Example 88 4-[(S)-N-[(R)-N'-isopropoxycarbonyl-phenylalanyl] prolyl) aminomethylbenzamidoxime (compound No. 395 of Table 1) NMR (CDCI3) 7.65 (br, 1 H), 7.53 (d, 2H), 7.29-7.19 (m, 8H), 5.89 (d, 2H), 5.01 (br, 2H), 4.58-4.45 (m, 4H), 4.27 (dd, 1 H), 3.65 (br, 1 H), 3.10-2.93 (m, 2H), 2.58 (q, 1 H), 2.17 (br, 1 H), 1.90-1.50 (m, 2H), 1.11 (d, 4H), 0.96 (d, 2H) IR: 3331, 2980, 2880, 2365, 1639, 1539, 1452, 126 Example 89 4-[(S)-N-[(R)-2-ethoxycarbonylamino-phenylacetyl} prolyl]
aminomethylbenzamidoxime (compound No. 403 of Table 1) NMR (CDC13) 7.80 (br, 1 H), 7.47 (d, 2H), 7.40-7.14 (m, 8H), 6.11 (dci, 1 H), 5.43 (dd, 1 H), 4.98 (br, 2H), 4.70-4.54 (m, 2H), 4.50-4.20 (m, 1 H), 4.15-4.00 (m, 1 H), 4.00-3.80 (m, 2H), 3.25-3.19 (rn, 1 H), 2.30-1.80 (m, 4H), 1.16 (dt, 3H) IR: 3339, 2980, 2365, 1641, 1524, 1437, 1385, 1057 Example 90 4-[(S)-N-[(R)-N'-ethoxycarbonyl-valyl]prolyl}
Example 87 4-[(S)-N-[(R)-2-hydroxy-cyclohexylacetyl] prolyl]
aminomethylbenzamidoxime (compound No. 391 of Table 1) NMR (DMSO-d6) 9.55 (br, 1 H), 8.31 (t, 1 H), 7.59 (d, 2H), 7.24 (d, 2H), 5.73 (br, 2H), 4.57 (m, 1 H), 4.26-4.32 (m, 3H), 3.91 (br, 1 H), 3.40-3.60 (m, 2H), 2.05-0.80 (m, 15H) IR: 3375, 2926, 2853, 1638, 1561, 1451, 1385, 1244 Example 88 4-[(S)-N-[(R)-N'-isopropoxycarbonyl-phenylalanyl] prolyl) aminomethylbenzamidoxime (compound No. 395 of Table 1) NMR (CDCI3) 7.65 (br, 1 H), 7.53 (d, 2H), 7.29-7.19 (m, 8H), 5.89 (d, 2H), 5.01 (br, 2H), 4.58-4.45 (m, 4H), 4.27 (dd, 1 H), 3.65 (br, 1 H), 3.10-2.93 (m, 2H), 2.58 (q, 1 H), 2.17 (br, 1 H), 1.90-1.50 (m, 2H), 1.11 (d, 4H), 0.96 (d, 2H) IR: 3331, 2980, 2880, 2365, 1639, 1539, 1452, 126 Example 89 4-[(S)-N-[(R)-2-ethoxycarbonylamino-phenylacetyl} prolyl]
aminomethylbenzamidoxime (compound No. 403 of Table 1) NMR (CDC13) 7.80 (br, 1 H), 7.47 (d, 2H), 7.40-7.14 (m, 8H), 6.11 (dci, 1 H), 5.43 (dd, 1 H), 4.98 (br, 2H), 4.70-4.54 (m, 2H), 4.50-4.20 (m, 1 H), 4.15-4.00 (m, 1 H), 4.00-3.80 (m, 2H), 3.25-3.19 (rn, 1 H), 2.30-1.80 (m, 4H), 1.16 (dt, 3H) IR: 3339, 2980, 2365, 1641, 1524, 1437, 1385, 1057 Example 90 4-[(S)-N-[(R)-N'-ethoxycarbonyl-valyl]prolyl}
aminomethylbenzamidoxime (compound No. 407 of Table 1) NMR (CDCI3) 7.57 (br, 1 H), 7.54 (d, 2H), 7.20 (d, 2H), 5.98 (d, 1 H), 4.97 (br, 2H), 4.68-4.59 (m, 2H), 4.24 (dd, 1 H), 4.07 (t, 1 H), 4.10-4.00 (m, 1 H), 3.90-3.80 (m, 1 H), 3.60-3.45 (m, 2H), 2.31 (br, 1H), 2.20-1.95 (m, 4H) 1.88 (d, '1 H), 1.01 (t, 3H), 0.97 (d, 6H) IR: 3337, 2971, 2878, 2363, 1640, 1539, 1445, 1277, 1238 Example 91 4-[(S)-N-[(R)-2-ethoxycarbonylamino-3,3-dimethylbutanoyl] prolyl]
aminomethylbenzamidoxime (compound No. 409 of Table 1) NMR (DMSO-d6) 8.01 (br, 1 H),7.59 (d, 2H), 7.21 (d, 2H), 7.19-7.15 (m, 1 H), 5.73 (br, 2H), 4.36-4.24 (m, 4H), 4.0-3.60 (m, 4H), 2.10-1.80 (m, 5H), 1.06 (t, 3H), 0.96 (s, 9H) IR: 3345, 2966, 2364, 1647, 1535, 1443, 1240 Example 92 4-[(S)-N-[(R)-2-ethoxycarbonylamino-heptanoyl) prol!yl]
aminomethylbenzamidoxime (compound No. 411 of Table 1) NMR (CDCI3) 7.63 (m, 1 H), 7.51 (d, 2H), 7.20 (d, 2H), 5.85 (d, 2H), 4.99 (br, 1 H), 4.67-4.58 (m, 2H), 4.35-4.28 (m, 2H), 3.99 (br, 1 H), 3.86-3.80 (m, 1 H), 3.58-3.50 (m, 2H), 2.31 (br, 1 H), 2.07-1.90 (m, 3H), 1.80-1.50 (m, 2H), 1.40-1.10 (m, 5H), 1.03 (t, 3H), 1.01-0.84 (m, 3H) IR: 3347, 2961, 2363, 2342, 1641, 1541, 1447, 1263, 1049 Example 93 4-[(S)-N-[(R)-2-t-butyloxycarbonylamino-heptanoyl] prolyl]
aminomethylbenzamidoxime (compound No. 412 of Table 1) NMR (CDCI3) 7.74-7.70 (m, 1 H), 7.49 (d, 2H), 7.27 (t, 1 H), 7.20 (d, 2H), 5.43 (d, 1 H), 4.93 (br, 2H), 4.65 (d, 1 H), 4.48-4.25 (m, 3H), 3.93 (br, 1 H), 3.50 (q, 1 H), 2.40-2.30 (m, 1 H), 2.10-1.90 (m, 3H), 1.70-1.50 (m, 2H), 1.42-1.21 (m, 13H), 0.92-0.80 (m, 3H) IR: 3337, 2961, 2934, 2363, 1641, 1535, 1449, 1368, 1165 Example 94 4-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl] prolyl]
aminomethylbenzamidoxime (compound No. 418 of Table 1) NMR (CDCl3) 7.58-7.51 (m, 1 H), 7.53 (d, 2H), 7.20 (d, 2H), 5.87 (d, '1 H), 5.01 (br, 2H), 4.64-4.56 (m, 2H), 4.40 (q, 1 H), 4.26 (dd, 1 H), 4.10-4.00 (m, 1 H), 3.84-3.78 (m, 1 H), 3.53-3.47 (m, 2H), 2.32 (br, 1 H), 2.10-1.90 (m, 3H), 1.61 (d, 2H), 1.00 (t, 3H), 0.97 (s, 9H) IR: 3324, 2957, 2263, 2342, 1642, 1541, 1445, 1248, 1059 Example 95 4-[(S)-N-[(R)-N'-(ethoxycarbonylmethyl)oxycarbonyl-phenylalanyl]
prolyl]aminomethylbenzamidoxime (compound No. 984 of Table 1) NMR (CDCI3) 7.54 (d, 2H), 7.41 (br, 1 H), 7.28-7.20 (m, 8H), 6.70 (d, 1 H), 5.09 (br, 2H), 4.66 (dd, 1 H), 4.60-4.55 (m, 2H), 4.22-4.00 (m, 4H), 4.03 (q, 2H), 3.62 (br, 1 H), 3.10-3.02 (m, 2H), 2.60-2.40 (m, 1 H), 2.14 (br, 1 H), 2.00-1.50 (m, 3H), 1.22 (t, 3H) IR: 3356, 3063, 2980, 2364, 1717, 1641, 1539, 1451, 1213, 702 Example 96 4-[(S)-N-[(R)-2-ethoxycarbonylamino-cyclohexylacetyl] prolyl]
aminomethylbenzamidoxime (compound No. 985 of Table 1) NMR (CDC13) 7.52 (d, 2H), 7.54-7.50 (m, 1 H), 7.20 (d, 2H), 6.03 (br, 1 H), 4.97 (br, 2H), 4.68 (q, 2H), 4.22 (dd, 1 H), 4.12-4.03 (m, 2H), 3.64-3.47 (m, 1 H), 3.20 (s, 3H), 2.32 (br, 1 H), 2.05-1.60 (m, 9H), 1.28-0.97 (m, 6H) IR: 3343, 2928, 2853, 2365, 1639, 1541, 1449, 1260 Example 97 4-[(S)-N-[(R)-2-ethoxycarbonylamino-2'-thienylacetyl] prolyl]
aminomethylbenzamidoxime (compound No. 986 of Table 1) NMR (CDCI3) 7.80-7.60 (m, 1 H), 7.46 (dd, 2H), 7.40-6.95 (m, 5H), 6.13 (dd, 1 H), 5.71 (dd, 1 H), 4.99 (br, 2H), 4.75-4.20 (m, 3H), 4.00-3.80 (m, 2H), 3.70-3.50 (m, 1 H),3.40-3.30 (m, 1 H), 2.40-1.80 (m, 4H), 1.16 (dt, 3H) IR: 3337, 2978, 2364, 1641, 1524, 1443, 1240, 1057, 710 Example 98 4-[(S)-N-[(R)-2-ethoxycarbonylamino-4'-fluorophenylacetyl] prolyl]
aminomethylbenzamidoxime (compound No. 987 of Table 1) NMR (CDCI3) 7.80 (t, 1 H), 7.46-7.27 (m, 4H), 7.19-6.92 (m, 4H), 6.19-6.15 (m, 1 H), 5.50 (dd, 1 H), 5.02 (br, 2H), 4.70-4.20 (m, 3H), 4.10-3.70 (m, 4H), 3.22-3.15 (m, 1 H), 2.25-1.80 (m, 4H), 1.16 (dt, 3H) IR: 3345, 3073, 2980, 2363, 2344, 1641, 1510, 1143 Example 99 4-[(S)-N-[(R)-N'-benzyloxycarbonyl-phenylalanyl] prolyl]
aminomethylbenzamidoxime (compound No. 988 of Table 1) NMR (CDC13) 7.50 (d, 2H), 7.49-7.30 (m, 1 H), 7.26-7.12 (m, 12H), 6,40-6.10 (m, 1 H), 4.85 (br, 2H), 4.90-4.70 (m, 1 H), 4.55-4.40 (m, 4H), 4.30-4.20 (m, 1 H), 3.70-3.60 (m, 1 H), 3.03-2.95 (m, 1 H), 2.20-2.15 (m, 1 H), 2.00-1.45 (m, 3H) Example 100 4-[(S)-N-(R)-2-t-butyloxycarbonylamino-4,4-dimethylpentanoyl] prolyl]
aminomethylbenzamidoxime (compound No. 989 of Table 1) 4'~4059~
NMR (CDCI3) 7.67 (t, 1 H), 7.53 (d, 2H), 7.22 (d, 2H), 5.34 (d, 1 H), 4.91 (br, 2H), 4.65 (d, 1 H), 4.42-4.34 (m, 3H), 4.00-3.90 (m, 1 H), 3.48 (q, 1 H), 2.40-2.30 (m, 1 H), 2.02-1.95 (m, 3H), 1.56-1.53 (m, 2H), 1.31 (s, 9H), 0.98 (s, 9H) IR: 3345, 2959, 2367, 1641, 1535, 1446, 1367, 1167 Example 101 4-[(S)-N-[(R)-N'-dimethylcarbamoyl-phenylalanyl] prolyl]
aminomethylbenzamidoxime (compound No. 990 of Table 1) NMR (DMSO-d6) 9.56 (s, 1 H), 8.11 (t, 1 H), 7.56 (d, 2H), 7.18 (d, 2H), 7.29-7.16 (m, 5H), 6.70 (d, 1 H), 5.74 (br, 2H), 4.40-4.05 (m, 4H), 2.94 (d, 2H), 2.93-2.70 (m, 2H), 2.60 (s, 6H), 1.90-1.60 (m, 4H) IR: 3306, 2932, 2880, 2363, 2341, 1634, 1541, 1453 Example 102 4-[(S)-N-[(S)-N'-benzyloxycarbonyl-f3-t-butylaspartyl] prolyl]
aminomethylbenzamidoxime (compound No. 991 of Table 1) NMR (CDCI3) 7.63 (br, 1 H), 7.51 (d, 2H), 7.33-7.26 (m, 5H), 7.18 (d, 2H), 6.07 (d, 1 H), 5.08 (dd, 2H), 4.92 (br, 2H), 4.90-4.70 (m, 1 H), 4.66 (d, 1 H), 4.40 (d, 2H), 3.90-3.80 (m, 2H), 3.0-2.90 (m, 1 H), 2.55 (dd, 1 H), 2.35-2.20 (m, 1 H), 2.08-1.90 (m, 3H), 1.25 (s, 9H) IR: 3364, 3063, 2978, 2363, 2343, 2343, 1717, 1641, 1539, 1450, 1369, 1253, Example 103 Trans-4-[(S)-N-[(R)-N'-ethoxycarbonyl-O-t-butoxy-seryl] prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 485 of Table 1) NMR (CDCI3) 7.16 (m, 1 H), 5.53 (m, 1 H), 4.60-4.53 (m, 2H), 4.47 (s, 2H), 4.13-4.06 (m, 2H), 3.76 (br, 2H), 3.60-3.50 (m, 2H), 3.07 (br, 2H), 2.41 (m, 2H), 2.04-1.20 (m, 12H), 1.27 (t, 3H), 1.16 (s, 9H), 1.03-0.94 (m, 2H) I R: 3352, 2930, 1701, 1651, 1541, 1448, 1259, 1053, 754 Example 104 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyi-O-t-butylseryl] prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 486 of Table 1) NMR (CDCI3) 7.19 (m, 1 H), 5.40 (d, 1 H), 4.87 (m, 1 H), 4.61-4..53 (m, 2H), 4.47 (br, 2H), 3.75 (m, 2H), 3.60-3.40 (m, 2H), 3.08 (t, 2H), 2.40 (m, 1 H), 2.20-1.20 (m, 12H), 1.21 (dd, 6H), 1.19 (s, 9H), 1.10-0.90 (m, 2H) IR: 3356, 2976, 1697, 1649, 1541, 1448, 1261, 1190, 1109, 1022 Example 105 Trans-4-[(S)-N-[(R)-N'-ethoxycarbonyl-O-t-(1',1'-dimethylpropyl]-seryl)prolyl]aminomethylcyclohexanecarboxamidoxime (cornpound No. 487 of Table 1) NMR (CDCI3) 7.14 (m, 1 H), 5.51 (d, 1 H), 4.60-4.50 (m, 2H), 4.48 (br, 2H), 4.09 (m, 2H), 3.78 (m, 2H), 3.55-3.45 (m, 2H), 3.06 (m, 2H), 2.35 (m, 1 H), 2.20-0.90 (m, 16H), 1.24 (t, 3H), 1.10 (s, 6H), 0.82 (t, 3H) IR: 3346, 2976, 2930, 1649, 1543, 1448, 1261, 1176, 1095, 1055 Example 106 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-(1',1'-ciimethylpropyl)-seryl] prolyl]aminomethylcyclohexanecarboxamidoxime (campound No. 488 of Table 1) NMR (CDCI3) 7.18 (m, 1 H), 5.38 (d, 1 H), 4.86 (m, 1 H), 4.61-4.50 (m, 2H), 4.47 (br, 2H), 3.77 (m, 2H), 3.57-3.42 (m, 2H), 3.06 (t, 2H), 2.39 (m, 1 H), 2.20-0.90 (m, 16H), 1.23 (dd, 6H), 1.10 (s, 6H), 0.82 (t, 3H) IR: 3346, 2976, 1703, 1651, 1541, 1448, 1263, 1178, 1109, 1030 Example 107 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-(1'-ethyl-1'-methyl-propyl)-seryl] prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 490 of Table 1) NMR (CDCI3) 7.17 (br, 1 H), 5.35 (br, 1 H), 4.86 (m, 1 H), 4.60-4.50 (rn, 2H), 4.47 (br, 2H), 3.78 (m, 2H), 3.53-3.38 (m, 2H), 3.07 (t, 2H), 2.37-1.20 (m, 17H), 1.23 (t, 6H), 1.06 (s, 3H), 1.06-0.82 (m, 2H), 0.79 (t, 6H) IR: 3350, 2976, 2932, 1651, 1541, 1450, 1375, 1263, 1109, 1026 Example 108 Trans-4-[(S)-N-[(R)-N'-ethoxycarbonyl-S-t-butyl-cystiriyl] prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 492 of Table 1) NMR (CDC13) 7.27 (m, 1 H), 5.81 (m, 1 H), 4.60-4.40 (m, 2H), 4.88 (br, 2H), 4.11 (m, 2H), 3.87 (m, 1 H), 3.68 (m, 1 H), 3.06 (m, 2H), 2.90-2.70 (m, 2H), 2.37 (m, 1 H), 2.10-1.20 (m, 12H), 1.32 (s, 9H), 1.25 (t, 3H), 1.10-0.90 (m, 2H) IR: 3346, 2930, 1699, 1649, 1541, 1448, 1257, 1163, 1051, 929 Example 109 Trans-4-[(S)-N-[(R)-2-ethoxycarbonylamino-3-isopropylthio-3-methyl-butanoyl] prolyl]aminomethylcyclohexanecarboxamidoxime (compound No.
497 of Table 1) NMR (CDCI3) 7.16 (m, 1 H), 5.62 (m, 1 H), 4.61 (d, 1 H), 4.47 (br, 2H), 4.35 (d, 1 H), 4.12 (m, 2H), 3.96 (m, 1 H), 3.76 (m, 1 H), 3.10 (m, 1 H), 3.00 (m, 2H), 2.38 (m, 1 H), 2.00-1.20 (m, 12H), 1.47 (s, 3H), 1.40 (s, 3H), 1.33-1.25 (m, 9H), 1.00-0.90 (m, 2H) IR: 3354, 2928, 1653, 1541, 1446, 1367, 1302, 1251, 1155, 1055 Example 110 Trans-4-[(S)-N-[(S)-N'-t-butyloxycarbonyl-seryl] prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 992 of Table 1) NMR (CDCI3) 7.76 (br, 1 H), 6.10 (br, 1 H), 5.40 (br, 1 H), 4.60 (br, 4H), 3.96 (br, 4H), 3.16-1.21 (m, 15H), 1.40 (s, 9H), 0.99 (br, 2H) IR: 3314, 2978, 1691, 1639, 1541, 1450, 1367, 1165, 1049 Example 111 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-t-butyl-threonyl] prolyi]
aminomethylcyclohexanecarboxamidoxime (compound No. 993 of Table 1) NMR (CDCI3) 7.24 (m, 1 H), 5.43 (d, 1 H), 4.85 (m, 1 H), 4.57 (d, 1 H), 4.47 (br, 2H), 4.23 (t, 1 H), 3.92 (t, 1 H), 3.80-3.70 (m, 2H), 3.06 (m, 2H), 2.36 (rri, 1 H), 2.00-1.20 (m, 12H), 1.23 (s, 9H) 1.23 (dd, 6H), 1.15 (d, 3H), 1.10-0.90 (m, 2H) I R: 3354, 2978, 1699, 1649, 1543, 1448, 1373, 1257, 1192, 1111, 1032 Example 112 Trans-4-[(S)-N-[(R)-2-acetoxy-cyclohexylacetyi] prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 994 of Table 1) NMR (CDCI3) 6.80 (br, 1 H), 4.61 (t, 2H), 4.49 (br, 2H), 3.90-3.84 (m, 1 H), 3.51-3.40 (m, 1 H), 3.10-2.85 (m, 2H), 2.38 (br, 1 H), 2.11 (s, 3H), 2.06-0.80 (m, 25H) IR: 3484, 3389, 2928, 2855, 1725, 1649, 1451, 1250 Example 113 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-(1'-methylcyclopentyl)-seryl] prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 995 of Table 1) NMR (CDC13) 7.18 (m, 1 H), 5.42 (m, 1 H), 4.85 (m, 2H), 4.60-4.49 (rn, 4H), 3.73 (m, 2H), 3.57-3.42 (m, 2H), 3.08 (m, 1 H), 2.40 (m, 1 H), 2.04-1.20 (mõ 21 H), 1.27-1.20 (m, 9H), 1.03-0.94 (m, 2H) I R: 3356, 2932, 1695, 1653, 1541, 1448, 1263, 1111, 1030, 918 According to the same procedures as that described in Example 48, the following compounds of Examples 114 to 122 were synthesized.
Example 114 Trans-4-[(S)-N-[(R)-2-t-butyloxycarbonylamino-4,4-dimethylpentanoyl]
prolyl]aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 533 of Table 1) NMR (CDC13) 7.14 (br, 1 H), 5.04 (d, 1 H), 4.74 (br, 1 H), 4.58 (d, 1 H), 4.40-4.30 (m, 1 H), 4.00-3.85 (m, 1 H), 3.94 (s, 3H), 3.46 (q, 1 H), 3.30-3.20 (m, 1 H), 2.95-2.88 (m, 1 H), 2.42 (br, 1 H), 2.26 (t, 1 H), 2.00-1.73 (m, 11 H), 1.54-1.26 (m, 4H), 1.43 (s, 9H), 1.00 (s, 9H) IR: 3347, 2955, 2870, 1765, 1645, 1539, 1443, 1254, 1169, 879 Example 115 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-Ieucyl] prolyl]
aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 540 of Table 1) NMR (CDCI3) 7.11 (br, 1 H), 5.18 (d, 1 H), 4.90-4.70 (m, 1 H), 4.77 (br, 2H), 4.56 (d, 1 H), 4.40-4.30 (m, 1 H), 3.95-3.86 (m, 1 H), 3.85 (s, 3H), 3.46 (q, 1 H), 3.20-2.95 (m, 2H), 2.40-2.30 (m, 1 H), 2.30-2.10 (m, 1 H), 2.00-1.20 (m, 13H), 1.23 (dd, 6H), 1.04-0.89 (m, 8H) IR: 3354, 2957, 2932, 2872, 2363, 2341, 1763, 1643, 1541, 1443, 1260 Example 116 Trans-4-[(S)-N-[(R)-N'-ethoxycarbonyl-O-t-butyl-seryl] prolyl]
aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 996 of Table 1) NMR (CDCI3) 7.20 (m, 1 H), 5.34 (m, 1 H), 4.70 (s, 2H), 4.61 (m, 1 H), 4.50 (m, 1 H), 4.12-4.06 (m, 2H), 3.85 (s, 3H), 3.74 (m, 2H), 3.60-3.39 (m, 2H), 3.06 (m, 2H), 2.41-1.20 (m, 13H), 1.25 (t, 3H), 1.16 (s, 9H), 1.08-0.94 (m, 2H) IR: 3348, 2976, 1768, 1703, 1645, 1541, 1442, 1255, 1053, 879, 752 Example 117 Trans-4-[(S)-N-[(R)-2-hydroxy-4-methyl-pentanoyl] prolyl]
aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 997 of Table 1) NMR (CDCI3) 7.07 (m, 1 H), 4.73 (br, 2H), 4.52 (d, 1 H), 4.23 (m, 4H), 3.56 (m, 1 H), 3.40 (m,1 H), 3.13 (m, 3H), 2.41 (m, 1 H), 2.30-0.90 (m, 15H), 1.33 (t, 3H), 0.97 (dd, 6H) IR: 3346, 2932, 1759, 1641, 1450, 1369, 1251, 1078, 920, 846 Example 118 Trans-4-[(S)-N-[(R)-N'-ethoxycarbonyl-O-t-butyl-seryl] prolyl]
aminomethylcyclohexanecarboxamide 0-acetyloxime (compound No. 998 of Table 1) NMR (CDCI3) 7.20 (m, 1 H), 5.33 (m, 1 H), 4.69 (s, 2H), 4.60 (m, 1 H), 4.51 (m, 1 H), 4.17-4.07 (m, 2H), 3.77-3.65 (m, 2H), 3.60-3.46 (m, 2H), 3.09-3.08 (m, 2H), 2.40-1.00 (m, 13H), 2.15 (s, 3H), 1.25 (t, 3H), 1.16 (s, 9H), 1.14-0.94 (rn, 2H) IR: 3346, 2976, 1641, 1541, 1448, 1234, 1053, 754 Example 119 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-t-butyl-seryl] prolyl]
aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 999 of Table 1) NMR (CDCI3) 7.23 (t, 1 H), 5.26 (d, 1 H), 4.85 (m, 1 H), 4.71 (m, 1 H), 4.59 (d, 1 H), 4.49 lr~~ld~e7q (m, 1 H), 3.85 (s, 3H), 3.73 (m, 2H), 3.61-3.49 (m, 2H), 3.06 (t, 2H), 2.36 (m, 1 H), 2.26 (t, 3H), 2.10-1.20 (m, 11H), 1.21 (dd, 6H), 1.16 (s, 9H), 1.10-0.90 (m, 2H) IR: 3348, 2978, 1768, 1703, 1649, 1541, 1444, 1259, 1192, 1109 Example 120 4-N-ethoxycarbonyi-amidino-[(S)-N-[(R)-2-methylsulfonylamino-4,4-dimethylpentanoyl] prolyl]aminomethylbenzene (compound No. 1000 of Table 1) NMR (CDCI3) 7.29 (d, 2H), 7.30 (d, 2H), 7.23 (t, 1 H), 5.53 (br, 1 H), 4.52-4.37 (m, 2H), 4.24-4.17 (m, 2H), 4.20 (q, 2H), 3.90-3.80 (m, 1 H), 3.50-3.40 (m, 1 H), 2.77 (s, 3H), 2.28-2.20 (m, 4H), 1.84 (br, 2H), 1.60-1.40 (m, 2H), 1.34 (t, 3H), 1.02 (s, 9H) IR: 3378, 2957, 2876, 2364, 2230, 1628, 1267, 1147 Example 121 4-N-methoxycarbonyl-amidino-[(S)-N-[(R)-2-methylsulfonylamino-cyclohexylacetyi] prolyl]aminomethylbenzene (compound No. 1001 of Table 1) NMR (CDCI3) 7.78 (d, 2H), 7.29 (d, 2H), 7.27 (t, 1 H), 5.49 (d, 1 H), 4,.56 (d, 1 H), 4.42 (dq, 2H), 3.77 (s, 3H), 3.80-3.70 (m, 2H), 3.60-3.51 (m, 1 H), 2.79 (s, 3H), 2.28-1.60 (m, 12H), 1.20-0.95 (m, 5H) IR: 3376, 2930, 2855, 2365, 1626, 1528, 1501, 1439, 1271, 1144 21.40598 Example 122 Trans-4-N-methoxycarbonyl-amidino-[(S)-N-[(R)-2-ethoxycarbonyl-amino-4,4-dimethylpentanoyl] prolyl] aminomethylcyclohexane (compound No.
599 of Table 1) NMR (CDCI3) 7.08 (br, 1 H), 5.17 (d, 1 H), 4.56 (d, 1 H), 4.50-4.40 (mõ 1 H), 4.20-3.80 (m, 3H), 3.70 (s, 3H), 3.47 (q, 1 H), 3.20-3.00 (m, 2H), 2.45-2.30 (m, 1 H), 2.20-1.30 (m, 15H), 1.24 (t, 3H), 0.99 (s, 9H), 1.10-0.89 (m, 2H) IR: 3366, 2953, 2365, 1780, 1697, 1640, 1533, 1441, 1271, 1055 According to the same procedures as that described in Example 52, the following compounds of Examples 123 to 125 were synthesized.
Example 123 Trans-4-amino-[(S)-N-[(R)-2-carboxymethylsulfonylamino-heptanoyl]
prolyl]aminomethylcyclohexane (compound No. 791 of Table 1) hydrochloride NMR (DMSO-d6) 7.97 (m, 2H), 7.57 (m, 1 H), 4.19 (m, 2H), 4.01 (d, 1 H), 3.80 (d, 1 H), 3.68 (m, 1 H), 3.50 (m, 1 H), 2.88 (m, 3H), 2.04 (m, 1 H), 1.90 (m, 5H), 1.73 (m, 4H), 1.58-1.13 (m, 12H), 1.00-0.84 (m, 5H) IR: 3387, 2934, 1726, 1637, 1553, 1452, 1325, 1159, 1090õ 1046, 604 Example 124 Trans-4-amino-[(S)-N-[(R)-N'-methylsulfonyl-O-methyltyrosyl] prolyl]
aminomethylcyclohexane (compound No. 1002 of Table 1) hydrochloride z14Q598 NMR (DMSO-d6) 8.10 (br, 3H), 7.77 (t, 1 H), 7.67 (d, 1 H), 7.17 (d, 2H), 6.87 (d, 2H), 4.25-4.16 (m, 1 H), 3.75 (br, 2H), 3.73 (s, 3H), 3.57-3.40 (m, 1 H), 3.00-2.70 (m, 5H), 2.77 (s, 3H), 2.00-1.71 (m, 8H), 1.40-1.20 (m, 3H), 1.00-0.80 (m, 2H) IR: 3385, 2936, 2363, 1639, 1514, 1450, 1304, 1248, 1149 Example 125 Trans-4-amino-[(S)-N-[(R)-N'-ethoxycarbonyl-0-t-butyloxy-seryl] prolyl]
aminomethylcyclohexane (compound No. 1003 of Table 1) hydrochloride NMR (DMSO-d6) 8.29 (s, 3H), 7.20 (s, 1 H), 5.69 (d, 1 H), 4.58-4.47 (m, 2H), 4.12 (m, 2H), 3.82 (m, 1 H), 3.61-3.48 (m, 2H), 3.09 (m, 2H), 2.32-0.86 (m, 15H), 1.27 (t, 3H), 1.16 (s, 9H) IR: 3358, 2974, 1645, 1541, 1448, 1257, 1192, 1053 According to the same procedures as that described in Example 67, the following compounds 126 to 130 were synthesized.
Example 126 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-[(S)-N-[(R)-2-hydroxy-cyclohexylacetyl] prolyl]aminomethylcyclohexane (compound No. 966 of Table 1) NMR (CDCI3) 7.08 (m, 1 H), 4.54 (d, 1 H), 4.06 (m, 1 H), 3.59 (m, 1 H), 3.49 (s, 2H), 3.46 (m, 1 H), 3.07 (m, 2H), 2.48 (m, 2H), 2.11 (s, 3H), 2.01 (m, 2H), 1.90-1.70 (m, 10H), 1.58 (m, 3H), 1.41-0.94 (m, 10H) IR: 3387, 2928, 2855, 1821, 1736, 1638, 1543, 1451, 1387, 1223, 1107, 999, Example 127 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-l[(S)-N-[(R)-N'-methylsulfonyl-phenylalanyl] prolyl]aminomethylcyclohexane (compound No.
967 of Table 1) NMR (CDCI3) 7.35-7.20 (m, 5H), 6.71 (t, 1 H), 5.48 (d, 1 H), 4.44 (m, 1 H), 4.25 (m, 1 H), 3.60 (m, 1 H), 3.48 (s, 2H), 3.09 (m, 1 H), 2.96 (m, 3H), 2.78 (s, 3H), 2.77 (m, 1 H), 2.50 (m, 1 H), 2.20 (m, 1 H), 2.11 (s, 3H), 1.88-1.56 (m, 8H), 1.42 (m, 1 H), 1.24 (m, 2H), 0.96 (m, 2H) IR: 3387, 2930, 1819, 1736, 1649, 1541, 1499, 1451, 1318, 1223, 1152, 999 Example 128 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-[(S)-N-[(R)-2-ethoxycarbonylamino-cyclohexylacetyl] prolyl]aminomethylcyclohexane (compound No. 1004 of Table 1) NMR (CDCI3) 7.11 (m, 1 H), 5.31 (m, 1 H), 4.58 (d, 1 H), 4.10 (t, 2H), 4.04 (m, 1 H), 3.94 (m, 1 H), 3.56 (m, 1 H), 3.49 (s, 2H), 3.04 (m, 2H), 2.52 (m, 1 H), 2.36 (m, 2H), 2.12 (s, 3H), 2.00 (m, 3H), 1.92-1.62 (m, 10H), 1.43 (m, 2H), 1.25 (q, 3H), 1.22 (m, 4H), 1.06 (m, 4H) IR: 3353, 2930, 2855, 1823, 1653, 1537, 1449, 1223, 1040, 999, 772, 627 Example 129 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-[(S)-N-[(R)-2-isopropoxyamino-4,4-dimethyl-pentanoyl] prolyl]aminomethylcyclohexane (compound No. 1005 of Table 1) NMR (CDCI3) 7.10 (m, 1 H), 5.07 (d, 1 H), 4.83 (m, 1 H), 4.57 (d, 1 H), 4.40 (m, 1 H), 3.96 (m, 1 H),3.48 (s, 2H), 3.45 (m, 2H), 3.04 (m, 2H), 2.50 (m, 1 H), 2.39 (m, 1 H), 2.11 (s, 3H), 2.00 (m, 3H), 1.83 (m, 3H), 1.69 (m, 5H), 1.57-1.42 (m, 3H), 1.25 (d, 3H), 1.22 (d, 3H), 1.00 (s, 9H) IR: 3349, 2934, 2872, 1823, 1653, 1537, 1445, 1225, 1047, 999, 712, 627 Example 130 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-[(S)-N-[( R)-2-methylsulfonylamino-cyclohexylacetyl] prolyl]aminomethylcyclohexane (compound No. 1006 of Table 1) NMR (CDCI3) 6.69 (t, 1 H), 5.26 (d, 1 H), 3.82 (m, 2H), 3.54 (m, 2H), 3.49 (s, 2H), 3.13 (m, 1 H), 3.00 (m, 1 H), 2.96 (s, 3H), 2.51 (m, 1 H), 2.30 (m, 1 H), 2.11 (s, 3H), 2.02 (m, 4H), 1.80 (m, 9H), 1.61 (m, 2H), 1.43 (m, 1 H), 1.20 (m, 5!H), 0.97 (m, 3H) IR: 3376, 2930, 2855, 1642, 1536, 1451, 1352, 1154, 984, 760, 619, 517 Experimental Example 1: Determination of antithrombiri activity (i) The measuring method for hydrolysis inhibition of synthetic substrate (S-2238) S-2238 (manufactured by Kabi Co.) is dissolved in a Tris hydrochloric acid buffer solution (pH: 8.3) to prepare a S-2238-0.4 M Tris hydrochloric acid solution having a concentration of 80 m. To 175 l of the solution, an aqueous solution of a compound of the present invention (515 l) is added.
After incubating at 37 C for one minute, 10 l of a bovine thrombin solution (4.4 units/ml, manufactured by Mochida Co., Ltd.) is added. A hydrolysis reaction rate of the substrate is determined by measuring a change in absorbance of 405 nm at 37 C.
The inhibitor concentration exhibiting an absorbance which is half as large as that obtained in case of adding no inhibitor (compound of the present invention) was determined as 150 ( m).
(ii) The measuring method for coagulation inhibition of rat plasma The compound of the present invention is dissolved in water or saline to form a solution of a total volume of 0.1 ml. To the solution, 0.1 ml of rat plasma is added and the mixture is incubated at 37 C for 30 seconds. Then, 0.1 mi of bovine thrombin (8 units/mI, Mochida Co., Ltd.) is added and the coagulation time is measured at 37 C. The concentration of the inhibitor (i.e., the compound of the present invention) which doubles the coagulation time that obtained in the absence of the inhibitor was determined as 150 ( m).
(iii) The measuring method for antithrombin activity of rat plasma on oral administration To a rat abstained from bait overnight, an aqueous solution or suspension of the present compound (inhibitor) (30 mg/kg) is orally administered using an oral sound.
After one hour, 2 ml of blood is collected from cava abdominalis and the antithrombin activity in plasma is measured using a method of the above item (ii). As a control experiment, the coagulation time of blood collected from a rat which has not been administered the inhibitor was measured. The extension effect on the coagulation time is represented by the numerical value obtained by comparing the data with those obtained in control experirnent, wherein the numerical value obtained in the control experiment was assumed to be 1.
Experimental Example 2: Determination of Antitrypsin activity (i) The measuring method for hydrolysis inhibition of synthetic substrate (S-2222) S-2222 (manufactured by Kabi Co.) is dissolved in a'Tris hydrochloric acid (pH: 8.3) to prepare a S-2222-0.4M Tris hydrochloric acid solution having a concentration of 400 m. To the solution (175 l), 515 l of a solution of a compound of the present invention is added. After incubating at 37'C for one minute, 10 l of a bovine trypsin solution (1 to 2 mg/ml, manufactured by Sigma Co.) is added. A hydrolysis reaction rate of the substrate is determined by measuring a change in absorbance of 405 nm at 37 C.
The inhibitor concentration exhibiting an absorbance which is half as large as that obtained in case of adding no inhibitor (compound of the present invention) was determined as 150 ( m).
The results are shown in Table 2.
aminomethylbenzamidoxime (compound No. 409 of Table 1) NMR (DMSO-d6) 8.01 (br, 1 H),7.59 (d, 2H), 7.21 (d, 2H), 7.19-7.15 (m, 1 H), 5.73 (br, 2H), 4.36-4.24 (m, 4H), 4.0-3.60 (m, 4H), 2.10-1.80 (m, 5H), 1.06 (t, 3H), 0.96 (s, 9H) IR: 3345, 2966, 2364, 1647, 1535, 1443, 1240 Example 92 4-[(S)-N-[(R)-2-ethoxycarbonylamino-heptanoyl) prol!yl]
aminomethylbenzamidoxime (compound No. 411 of Table 1) NMR (CDCI3) 7.63 (m, 1 H), 7.51 (d, 2H), 7.20 (d, 2H), 5.85 (d, 2H), 4.99 (br, 1 H), 4.67-4.58 (m, 2H), 4.35-4.28 (m, 2H), 3.99 (br, 1 H), 3.86-3.80 (m, 1 H), 3.58-3.50 (m, 2H), 2.31 (br, 1 H), 2.07-1.90 (m, 3H), 1.80-1.50 (m, 2H), 1.40-1.10 (m, 5H), 1.03 (t, 3H), 1.01-0.84 (m, 3H) IR: 3347, 2961, 2363, 2342, 1641, 1541, 1447, 1263, 1049 Example 93 4-[(S)-N-[(R)-2-t-butyloxycarbonylamino-heptanoyl] prolyl]
aminomethylbenzamidoxime (compound No. 412 of Table 1) NMR (CDCI3) 7.74-7.70 (m, 1 H), 7.49 (d, 2H), 7.27 (t, 1 H), 7.20 (d, 2H), 5.43 (d, 1 H), 4.93 (br, 2H), 4.65 (d, 1 H), 4.48-4.25 (m, 3H), 3.93 (br, 1 H), 3.50 (q, 1 H), 2.40-2.30 (m, 1 H), 2.10-1.90 (m, 3H), 1.70-1.50 (m, 2H), 1.42-1.21 (m, 13H), 0.92-0.80 (m, 3H) IR: 3337, 2961, 2934, 2363, 1641, 1535, 1449, 1368, 1165 Example 94 4-[(S)-N-[(R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl] prolyl]
aminomethylbenzamidoxime (compound No. 418 of Table 1) NMR (CDCl3) 7.58-7.51 (m, 1 H), 7.53 (d, 2H), 7.20 (d, 2H), 5.87 (d, '1 H), 5.01 (br, 2H), 4.64-4.56 (m, 2H), 4.40 (q, 1 H), 4.26 (dd, 1 H), 4.10-4.00 (m, 1 H), 3.84-3.78 (m, 1 H), 3.53-3.47 (m, 2H), 2.32 (br, 1 H), 2.10-1.90 (m, 3H), 1.61 (d, 2H), 1.00 (t, 3H), 0.97 (s, 9H) IR: 3324, 2957, 2263, 2342, 1642, 1541, 1445, 1248, 1059 Example 95 4-[(S)-N-[(R)-N'-(ethoxycarbonylmethyl)oxycarbonyl-phenylalanyl]
prolyl]aminomethylbenzamidoxime (compound No. 984 of Table 1) NMR (CDCI3) 7.54 (d, 2H), 7.41 (br, 1 H), 7.28-7.20 (m, 8H), 6.70 (d, 1 H), 5.09 (br, 2H), 4.66 (dd, 1 H), 4.60-4.55 (m, 2H), 4.22-4.00 (m, 4H), 4.03 (q, 2H), 3.62 (br, 1 H), 3.10-3.02 (m, 2H), 2.60-2.40 (m, 1 H), 2.14 (br, 1 H), 2.00-1.50 (m, 3H), 1.22 (t, 3H) IR: 3356, 3063, 2980, 2364, 1717, 1641, 1539, 1451, 1213, 702 Example 96 4-[(S)-N-[(R)-2-ethoxycarbonylamino-cyclohexylacetyl] prolyl]
aminomethylbenzamidoxime (compound No. 985 of Table 1) NMR (CDC13) 7.52 (d, 2H), 7.54-7.50 (m, 1 H), 7.20 (d, 2H), 6.03 (br, 1 H), 4.97 (br, 2H), 4.68 (q, 2H), 4.22 (dd, 1 H), 4.12-4.03 (m, 2H), 3.64-3.47 (m, 1 H), 3.20 (s, 3H), 2.32 (br, 1 H), 2.05-1.60 (m, 9H), 1.28-0.97 (m, 6H) IR: 3343, 2928, 2853, 2365, 1639, 1541, 1449, 1260 Example 97 4-[(S)-N-[(R)-2-ethoxycarbonylamino-2'-thienylacetyl] prolyl]
aminomethylbenzamidoxime (compound No. 986 of Table 1) NMR (CDCI3) 7.80-7.60 (m, 1 H), 7.46 (dd, 2H), 7.40-6.95 (m, 5H), 6.13 (dd, 1 H), 5.71 (dd, 1 H), 4.99 (br, 2H), 4.75-4.20 (m, 3H), 4.00-3.80 (m, 2H), 3.70-3.50 (m, 1 H),3.40-3.30 (m, 1 H), 2.40-1.80 (m, 4H), 1.16 (dt, 3H) IR: 3337, 2978, 2364, 1641, 1524, 1443, 1240, 1057, 710 Example 98 4-[(S)-N-[(R)-2-ethoxycarbonylamino-4'-fluorophenylacetyl] prolyl]
aminomethylbenzamidoxime (compound No. 987 of Table 1) NMR (CDCI3) 7.80 (t, 1 H), 7.46-7.27 (m, 4H), 7.19-6.92 (m, 4H), 6.19-6.15 (m, 1 H), 5.50 (dd, 1 H), 5.02 (br, 2H), 4.70-4.20 (m, 3H), 4.10-3.70 (m, 4H), 3.22-3.15 (m, 1 H), 2.25-1.80 (m, 4H), 1.16 (dt, 3H) IR: 3345, 3073, 2980, 2363, 2344, 1641, 1510, 1143 Example 99 4-[(S)-N-[(R)-N'-benzyloxycarbonyl-phenylalanyl] prolyl]
aminomethylbenzamidoxime (compound No. 988 of Table 1) NMR (CDC13) 7.50 (d, 2H), 7.49-7.30 (m, 1 H), 7.26-7.12 (m, 12H), 6,40-6.10 (m, 1 H), 4.85 (br, 2H), 4.90-4.70 (m, 1 H), 4.55-4.40 (m, 4H), 4.30-4.20 (m, 1 H), 3.70-3.60 (m, 1 H), 3.03-2.95 (m, 1 H), 2.20-2.15 (m, 1 H), 2.00-1.45 (m, 3H) Example 100 4-[(S)-N-(R)-2-t-butyloxycarbonylamino-4,4-dimethylpentanoyl] prolyl]
aminomethylbenzamidoxime (compound No. 989 of Table 1) 4'~4059~
NMR (CDCI3) 7.67 (t, 1 H), 7.53 (d, 2H), 7.22 (d, 2H), 5.34 (d, 1 H), 4.91 (br, 2H), 4.65 (d, 1 H), 4.42-4.34 (m, 3H), 4.00-3.90 (m, 1 H), 3.48 (q, 1 H), 2.40-2.30 (m, 1 H), 2.02-1.95 (m, 3H), 1.56-1.53 (m, 2H), 1.31 (s, 9H), 0.98 (s, 9H) IR: 3345, 2959, 2367, 1641, 1535, 1446, 1367, 1167 Example 101 4-[(S)-N-[(R)-N'-dimethylcarbamoyl-phenylalanyl] prolyl]
aminomethylbenzamidoxime (compound No. 990 of Table 1) NMR (DMSO-d6) 9.56 (s, 1 H), 8.11 (t, 1 H), 7.56 (d, 2H), 7.18 (d, 2H), 7.29-7.16 (m, 5H), 6.70 (d, 1 H), 5.74 (br, 2H), 4.40-4.05 (m, 4H), 2.94 (d, 2H), 2.93-2.70 (m, 2H), 2.60 (s, 6H), 1.90-1.60 (m, 4H) IR: 3306, 2932, 2880, 2363, 2341, 1634, 1541, 1453 Example 102 4-[(S)-N-[(S)-N'-benzyloxycarbonyl-f3-t-butylaspartyl] prolyl]
aminomethylbenzamidoxime (compound No. 991 of Table 1) NMR (CDCI3) 7.63 (br, 1 H), 7.51 (d, 2H), 7.33-7.26 (m, 5H), 7.18 (d, 2H), 6.07 (d, 1 H), 5.08 (dd, 2H), 4.92 (br, 2H), 4.90-4.70 (m, 1 H), 4.66 (d, 1 H), 4.40 (d, 2H), 3.90-3.80 (m, 2H), 3.0-2.90 (m, 1 H), 2.55 (dd, 1 H), 2.35-2.20 (m, 1 H), 2.08-1.90 (m, 3H), 1.25 (s, 9H) IR: 3364, 3063, 2978, 2363, 2343, 2343, 1717, 1641, 1539, 1450, 1369, 1253, Example 103 Trans-4-[(S)-N-[(R)-N'-ethoxycarbonyl-O-t-butoxy-seryl] prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 485 of Table 1) NMR (CDCI3) 7.16 (m, 1 H), 5.53 (m, 1 H), 4.60-4.53 (m, 2H), 4.47 (s, 2H), 4.13-4.06 (m, 2H), 3.76 (br, 2H), 3.60-3.50 (m, 2H), 3.07 (br, 2H), 2.41 (m, 2H), 2.04-1.20 (m, 12H), 1.27 (t, 3H), 1.16 (s, 9H), 1.03-0.94 (m, 2H) I R: 3352, 2930, 1701, 1651, 1541, 1448, 1259, 1053, 754 Example 104 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyi-O-t-butylseryl] prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 486 of Table 1) NMR (CDCI3) 7.19 (m, 1 H), 5.40 (d, 1 H), 4.87 (m, 1 H), 4.61-4..53 (m, 2H), 4.47 (br, 2H), 3.75 (m, 2H), 3.60-3.40 (m, 2H), 3.08 (t, 2H), 2.40 (m, 1 H), 2.20-1.20 (m, 12H), 1.21 (dd, 6H), 1.19 (s, 9H), 1.10-0.90 (m, 2H) IR: 3356, 2976, 1697, 1649, 1541, 1448, 1261, 1190, 1109, 1022 Example 105 Trans-4-[(S)-N-[(R)-N'-ethoxycarbonyl-O-t-(1',1'-dimethylpropyl]-seryl)prolyl]aminomethylcyclohexanecarboxamidoxime (cornpound No. 487 of Table 1) NMR (CDCI3) 7.14 (m, 1 H), 5.51 (d, 1 H), 4.60-4.50 (m, 2H), 4.48 (br, 2H), 4.09 (m, 2H), 3.78 (m, 2H), 3.55-3.45 (m, 2H), 3.06 (m, 2H), 2.35 (m, 1 H), 2.20-0.90 (m, 16H), 1.24 (t, 3H), 1.10 (s, 6H), 0.82 (t, 3H) IR: 3346, 2976, 2930, 1649, 1543, 1448, 1261, 1176, 1095, 1055 Example 106 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-(1',1'-ciimethylpropyl)-seryl] prolyl]aminomethylcyclohexanecarboxamidoxime (campound No. 488 of Table 1) NMR (CDCI3) 7.18 (m, 1 H), 5.38 (d, 1 H), 4.86 (m, 1 H), 4.61-4.50 (m, 2H), 4.47 (br, 2H), 3.77 (m, 2H), 3.57-3.42 (m, 2H), 3.06 (t, 2H), 2.39 (m, 1 H), 2.20-0.90 (m, 16H), 1.23 (dd, 6H), 1.10 (s, 6H), 0.82 (t, 3H) IR: 3346, 2976, 1703, 1651, 1541, 1448, 1263, 1178, 1109, 1030 Example 107 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-(1'-ethyl-1'-methyl-propyl)-seryl] prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 490 of Table 1) NMR (CDCI3) 7.17 (br, 1 H), 5.35 (br, 1 H), 4.86 (m, 1 H), 4.60-4.50 (rn, 2H), 4.47 (br, 2H), 3.78 (m, 2H), 3.53-3.38 (m, 2H), 3.07 (t, 2H), 2.37-1.20 (m, 17H), 1.23 (t, 6H), 1.06 (s, 3H), 1.06-0.82 (m, 2H), 0.79 (t, 6H) IR: 3350, 2976, 2932, 1651, 1541, 1450, 1375, 1263, 1109, 1026 Example 108 Trans-4-[(S)-N-[(R)-N'-ethoxycarbonyl-S-t-butyl-cystiriyl] prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 492 of Table 1) NMR (CDC13) 7.27 (m, 1 H), 5.81 (m, 1 H), 4.60-4.40 (m, 2H), 4.88 (br, 2H), 4.11 (m, 2H), 3.87 (m, 1 H), 3.68 (m, 1 H), 3.06 (m, 2H), 2.90-2.70 (m, 2H), 2.37 (m, 1 H), 2.10-1.20 (m, 12H), 1.32 (s, 9H), 1.25 (t, 3H), 1.10-0.90 (m, 2H) IR: 3346, 2930, 1699, 1649, 1541, 1448, 1257, 1163, 1051, 929 Example 109 Trans-4-[(S)-N-[(R)-2-ethoxycarbonylamino-3-isopropylthio-3-methyl-butanoyl] prolyl]aminomethylcyclohexanecarboxamidoxime (compound No.
497 of Table 1) NMR (CDCI3) 7.16 (m, 1 H), 5.62 (m, 1 H), 4.61 (d, 1 H), 4.47 (br, 2H), 4.35 (d, 1 H), 4.12 (m, 2H), 3.96 (m, 1 H), 3.76 (m, 1 H), 3.10 (m, 1 H), 3.00 (m, 2H), 2.38 (m, 1 H), 2.00-1.20 (m, 12H), 1.47 (s, 3H), 1.40 (s, 3H), 1.33-1.25 (m, 9H), 1.00-0.90 (m, 2H) IR: 3354, 2928, 1653, 1541, 1446, 1367, 1302, 1251, 1155, 1055 Example 110 Trans-4-[(S)-N-[(S)-N'-t-butyloxycarbonyl-seryl] prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 992 of Table 1) NMR (CDCI3) 7.76 (br, 1 H), 6.10 (br, 1 H), 5.40 (br, 1 H), 4.60 (br, 4H), 3.96 (br, 4H), 3.16-1.21 (m, 15H), 1.40 (s, 9H), 0.99 (br, 2H) IR: 3314, 2978, 1691, 1639, 1541, 1450, 1367, 1165, 1049 Example 111 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-t-butyl-threonyl] prolyi]
aminomethylcyclohexanecarboxamidoxime (compound No. 993 of Table 1) NMR (CDCI3) 7.24 (m, 1 H), 5.43 (d, 1 H), 4.85 (m, 1 H), 4.57 (d, 1 H), 4.47 (br, 2H), 4.23 (t, 1 H), 3.92 (t, 1 H), 3.80-3.70 (m, 2H), 3.06 (m, 2H), 2.36 (rri, 1 H), 2.00-1.20 (m, 12H), 1.23 (s, 9H) 1.23 (dd, 6H), 1.15 (d, 3H), 1.10-0.90 (m, 2H) I R: 3354, 2978, 1699, 1649, 1543, 1448, 1373, 1257, 1192, 1111, 1032 Example 112 Trans-4-[(S)-N-[(R)-2-acetoxy-cyclohexylacetyi] prolyl]
aminomethylcyclohexanecarboxamidoxime (compound No. 994 of Table 1) NMR (CDCI3) 6.80 (br, 1 H), 4.61 (t, 2H), 4.49 (br, 2H), 3.90-3.84 (m, 1 H), 3.51-3.40 (m, 1 H), 3.10-2.85 (m, 2H), 2.38 (br, 1 H), 2.11 (s, 3H), 2.06-0.80 (m, 25H) IR: 3484, 3389, 2928, 2855, 1725, 1649, 1451, 1250 Example 113 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-(1'-methylcyclopentyl)-seryl] prolyl]aminomethylcyclohexanecarboxamidoxime (compound No. 995 of Table 1) NMR (CDC13) 7.18 (m, 1 H), 5.42 (m, 1 H), 4.85 (m, 2H), 4.60-4.49 (rn, 4H), 3.73 (m, 2H), 3.57-3.42 (m, 2H), 3.08 (m, 1 H), 2.40 (m, 1 H), 2.04-1.20 (mõ 21 H), 1.27-1.20 (m, 9H), 1.03-0.94 (m, 2H) I R: 3356, 2932, 1695, 1653, 1541, 1448, 1263, 1111, 1030, 918 According to the same procedures as that described in Example 48, the following compounds of Examples 114 to 122 were synthesized.
Example 114 Trans-4-[(S)-N-[(R)-2-t-butyloxycarbonylamino-4,4-dimethylpentanoyl]
prolyl]aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 533 of Table 1) NMR (CDC13) 7.14 (br, 1 H), 5.04 (d, 1 H), 4.74 (br, 1 H), 4.58 (d, 1 H), 4.40-4.30 (m, 1 H), 4.00-3.85 (m, 1 H), 3.94 (s, 3H), 3.46 (q, 1 H), 3.30-3.20 (m, 1 H), 2.95-2.88 (m, 1 H), 2.42 (br, 1 H), 2.26 (t, 1 H), 2.00-1.73 (m, 11 H), 1.54-1.26 (m, 4H), 1.43 (s, 9H), 1.00 (s, 9H) IR: 3347, 2955, 2870, 1765, 1645, 1539, 1443, 1254, 1169, 879 Example 115 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-Ieucyl] prolyl]
aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 540 of Table 1) NMR (CDCI3) 7.11 (br, 1 H), 5.18 (d, 1 H), 4.90-4.70 (m, 1 H), 4.77 (br, 2H), 4.56 (d, 1 H), 4.40-4.30 (m, 1 H), 3.95-3.86 (m, 1 H), 3.85 (s, 3H), 3.46 (q, 1 H), 3.20-2.95 (m, 2H), 2.40-2.30 (m, 1 H), 2.30-2.10 (m, 1 H), 2.00-1.20 (m, 13H), 1.23 (dd, 6H), 1.04-0.89 (m, 8H) IR: 3354, 2957, 2932, 2872, 2363, 2341, 1763, 1643, 1541, 1443, 1260 Example 116 Trans-4-[(S)-N-[(R)-N'-ethoxycarbonyl-O-t-butyl-seryl] prolyl]
aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 996 of Table 1) NMR (CDCI3) 7.20 (m, 1 H), 5.34 (m, 1 H), 4.70 (s, 2H), 4.61 (m, 1 H), 4.50 (m, 1 H), 4.12-4.06 (m, 2H), 3.85 (s, 3H), 3.74 (m, 2H), 3.60-3.39 (m, 2H), 3.06 (m, 2H), 2.41-1.20 (m, 13H), 1.25 (t, 3H), 1.16 (s, 9H), 1.08-0.94 (m, 2H) IR: 3348, 2976, 1768, 1703, 1645, 1541, 1442, 1255, 1053, 879, 752 Example 117 Trans-4-[(S)-N-[(R)-2-hydroxy-4-methyl-pentanoyl] prolyl]
aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 997 of Table 1) NMR (CDCI3) 7.07 (m, 1 H), 4.73 (br, 2H), 4.52 (d, 1 H), 4.23 (m, 4H), 3.56 (m, 1 H), 3.40 (m,1 H), 3.13 (m, 3H), 2.41 (m, 1 H), 2.30-0.90 (m, 15H), 1.33 (t, 3H), 0.97 (dd, 6H) IR: 3346, 2932, 1759, 1641, 1450, 1369, 1251, 1078, 920, 846 Example 118 Trans-4-[(S)-N-[(R)-N'-ethoxycarbonyl-O-t-butyl-seryl] prolyl]
aminomethylcyclohexanecarboxamide 0-acetyloxime (compound No. 998 of Table 1) NMR (CDCI3) 7.20 (m, 1 H), 5.33 (m, 1 H), 4.69 (s, 2H), 4.60 (m, 1 H), 4.51 (m, 1 H), 4.17-4.07 (m, 2H), 3.77-3.65 (m, 2H), 3.60-3.46 (m, 2H), 3.09-3.08 (m, 2H), 2.40-1.00 (m, 13H), 2.15 (s, 3H), 1.25 (t, 3H), 1.16 (s, 9H), 1.14-0.94 (rn, 2H) IR: 3346, 2976, 1641, 1541, 1448, 1234, 1053, 754 Example 119 Trans-4-[(S)-N-[(R)-N'-isopropoxycarbonyl-O-t-butyl-seryl] prolyl]
aminomethylcyclohexanecarboxamide 0-methoxycarbonyloxime (compound No. 999 of Table 1) NMR (CDCI3) 7.23 (t, 1 H), 5.26 (d, 1 H), 4.85 (m, 1 H), 4.71 (m, 1 H), 4.59 (d, 1 H), 4.49 lr~~ld~e7q (m, 1 H), 3.85 (s, 3H), 3.73 (m, 2H), 3.61-3.49 (m, 2H), 3.06 (t, 2H), 2.36 (m, 1 H), 2.26 (t, 3H), 2.10-1.20 (m, 11H), 1.21 (dd, 6H), 1.16 (s, 9H), 1.10-0.90 (m, 2H) IR: 3348, 2978, 1768, 1703, 1649, 1541, 1444, 1259, 1192, 1109 Example 120 4-N-ethoxycarbonyi-amidino-[(S)-N-[(R)-2-methylsulfonylamino-4,4-dimethylpentanoyl] prolyl]aminomethylbenzene (compound No. 1000 of Table 1) NMR (CDCI3) 7.29 (d, 2H), 7.30 (d, 2H), 7.23 (t, 1 H), 5.53 (br, 1 H), 4.52-4.37 (m, 2H), 4.24-4.17 (m, 2H), 4.20 (q, 2H), 3.90-3.80 (m, 1 H), 3.50-3.40 (m, 1 H), 2.77 (s, 3H), 2.28-2.20 (m, 4H), 1.84 (br, 2H), 1.60-1.40 (m, 2H), 1.34 (t, 3H), 1.02 (s, 9H) IR: 3378, 2957, 2876, 2364, 2230, 1628, 1267, 1147 Example 121 4-N-methoxycarbonyl-amidino-[(S)-N-[(R)-2-methylsulfonylamino-cyclohexylacetyi] prolyl]aminomethylbenzene (compound No. 1001 of Table 1) NMR (CDCI3) 7.78 (d, 2H), 7.29 (d, 2H), 7.27 (t, 1 H), 5.49 (d, 1 H), 4,.56 (d, 1 H), 4.42 (dq, 2H), 3.77 (s, 3H), 3.80-3.70 (m, 2H), 3.60-3.51 (m, 1 H), 2.79 (s, 3H), 2.28-1.60 (m, 12H), 1.20-0.95 (m, 5H) IR: 3376, 2930, 2855, 2365, 1626, 1528, 1501, 1439, 1271, 1144 21.40598 Example 122 Trans-4-N-methoxycarbonyl-amidino-[(S)-N-[(R)-2-ethoxycarbonyl-amino-4,4-dimethylpentanoyl] prolyl] aminomethylcyclohexane (compound No.
599 of Table 1) NMR (CDCI3) 7.08 (br, 1 H), 5.17 (d, 1 H), 4.56 (d, 1 H), 4.50-4.40 (mõ 1 H), 4.20-3.80 (m, 3H), 3.70 (s, 3H), 3.47 (q, 1 H), 3.20-3.00 (m, 2H), 2.45-2.30 (m, 1 H), 2.20-1.30 (m, 15H), 1.24 (t, 3H), 0.99 (s, 9H), 1.10-0.89 (m, 2H) IR: 3366, 2953, 2365, 1780, 1697, 1640, 1533, 1441, 1271, 1055 According to the same procedures as that described in Example 52, the following compounds of Examples 123 to 125 were synthesized.
Example 123 Trans-4-amino-[(S)-N-[(R)-2-carboxymethylsulfonylamino-heptanoyl]
prolyl]aminomethylcyclohexane (compound No. 791 of Table 1) hydrochloride NMR (DMSO-d6) 7.97 (m, 2H), 7.57 (m, 1 H), 4.19 (m, 2H), 4.01 (d, 1 H), 3.80 (d, 1 H), 3.68 (m, 1 H), 3.50 (m, 1 H), 2.88 (m, 3H), 2.04 (m, 1 H), 1.90 (m, 5H), 1.73 (m, 4H), 1.58-1.13 (m, 12H), 1.00-0.84 (m, 5H) IR: 3387, 2934, 1726, 1637, 1553, 1452, 1325, 1159, 1090õ 1046, 604 Example 124 Trans-4-amino-[(S)-N-[(R)-N'-methylsulfonyl-O-methyltyrosyl] prolyl]
aminomethylcyclohexane (compound No. 1002 of Table 1) hydrochloride z14Q598 NMR (DMSO-d6) 8.10 (br, 3H), 7.77 (t, 1 H), 7.67 (d, 1 H), 7.17 (d, 2H), 6.87 (d, 2H), 4.25-4.16 (m, 1 H), 3.75 (br, 2H), 3.73 (s, 3H), 3.57-3.40 (m, 1 H), 3.00-2.70 (m, 5H), 2.77 (s, 3H), 2.00-1.71 (m, 8H), 1.40-1.20 (m, 3H), 1.00-0.80 (m, 2H) IR: 3385, 2936, 2363, 1639, 1514, 1450, 1304, 1248, 1149 Example 125 Trans-4-amino-[(S)-N-[(R)-N'-ethoxycarbonyl-0-t-butyloxy-seryl] prolyl]
aminomethylcyclohexane (compound No. 1003 of Table 1) hydrochloride NMR (DMSO-d6) 8.29 (s, 3H), 7.20 (s, 1 H), 5.69 (d, 1 H), 4.58-4.47 (m, 2H), 4.12 (m, 2H), 3.82 (m, 1 H), 3.61-3.48 (m, 2H), 3.09 (m, 2H), 2.32-0.86 (m, 15H), 1.27 (t, 3H), 1.16 (s, 9H) IR: 3358, 2974, 1645, 1541, 1448, 1257, 1192, 1053 According to the same procedures as that described in Example 67, the following compounds 126 to 130 were synthesized.
Example 126 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-[(S)-N-[(R)-2-hydroxy-cyclohexylacetyl] prolyl]aminomethylcyclohexane (compound No. 966 of Table 1) NMR (CDCI3) 7.08 (m, 1 H), 4.54 (d, 1 H), 4.06 (m, 1 H), 3.59 (m, 1 H), 3.49 (s, 2H), 3.46 (m, 1 H), 3.07 (m, 2H), 2.48 (m, 2H), 2.11 (s, 3H), 2.01 (m, 2H), 1.90-1.70 (m, 10H), 1.58 (m, 3H), 1.41-0.94 (m, 10H) IR: 3387, 2928, 2855, 1821, 1736, 1638, 1543, 1451, 1387, 1223, 1107, 999, Example 127 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-l[(S)-N-[(R)-N'-methylsulfonyl-phenylalanyl] prolyl]aminomethylcyclohexane (compound No.
967 of Table 1) NMR (CDCI3) 7.35-7.20 (m, 5H), 6.71 (t, 1 H), 5.48 (d, 1 H), 4.44 (m, 1 H), 4.25 (m, 1 H), 3.60 (m, 1 H), 3.48 (s, 2H), 3.09 (m, 1 H), 2.96 (m, 3H), 2.78 (s, 3H), 2.77 (m, 1 H), 2.50 (m, 1 H), 2.20 (m, 1 H), 2.11 (s, 3H), 1.88-1.56 (m, 8H), 1.42 (m, 1 H), 1.24 (m, 2H), 0.96 (m, 2H) IR: 3387, 2930, 1819, 1736, 1649, 1541, 1499, 1451, 1318, 1223, 1152, 999 Example 128 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-[(S)-N-[(R)-2-ethoxycarbonylamino-cyclohexylacetyl] prolyl]aminomethylcyclohexane (compound No. 1004 of Table 1) NMR (CDCI3) 7.11 (m, 1 H), 5.31 (m, 1 H), 4.58 (d, 1 H), 4.10 (t, 2H), 4.04 (m, 1 H), 3.94 (m, 1 H), 3.56 (m, 1 H), 3.49 (s, 2H), 3.04 (m, 2H), 2.52 (m, 1 H), 2.36 (m, 2H), 2.12 (s, 3H), 2.00 (m, 3H), 1.92-1.62 (m, 10H), 1.43 (m, 2H), 1.25 (q, 3H), 1.22 (m, 4H), 1.06 (m, 4H) IR: 3353, 2930, 2855, 1823, 1653, 1537, 1449, 1223, 1040, 999, 772, 627 Example 129 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-[(S)-N-[(R)-2-isopropoxyamino-4,4-dimethyl-pentanoyl] prolyl]aminomethylcyclohexane (compound No. 1005 of Table 1) NMR (CDCI3) 7.10 (m, 1 H), 5.07 (d, 1 H), 4.83 (m, 1 H), 4.57 (d, 1 H), 4.40 (m, 1 H), 3.96 (m, 1 H),3.48 (s, 2H), 3.45 (m, 2H), 3.04 (m, 2H), 2.50 (m, 1 H), 2.39 (m, 1 H), 2.11 (s, 3H), 2.00 (m, 3H), 1.83 (m, 3H), 1.69 (m, 5H), 1.57-1.42 (m, 3H), 1.25 (d, 3H), 1.22 (d, 3H), 1.00 (s, 9H) IR: 3349, 2934, 2872, 1823, 1653, 1537, 1445, 1225, 1047, 999, 712, 627 Example 130 Trans-4-(5-methyl-1,3-dioxo-2-on-4-ylmethyl)amino-[(S)-N-[( R)-2-methylsulfonylamino-cyclohexylacetyl] prolyl]aminomethylcyclohexane (compound No. 1006 of Table 1) NMR (CDCI3) 6.69 (t, 1 H), 5.26 (d, 1 H), 3.82 (m, 2H), 3.54 (m, 2H), 3.49 (s, 2H), 3.13 (m, 1 H), 3.00 (m, 1 H), 2.96 (s, 3H), 2.51 (m, 1 H), 2.30 (m, 1 H), 2.11 (s, 3H), 2.02 (m, 4H), 1.80 (m, 9H), 1.61 (m, 2H), 1.43 (m, 1 H), 1.20 (m, 5!H), 0.97 (m, 3H) IR: 3376, 2930, 2855, 1642, 1536, 1451, 1352, 1154, 984, 760, 619, 517 Experimental Example 1: Determination of antithrombiri activity (i) The measuring method for hydrolysis inhibition of synthetic substrate (S-2238) S-2238 (manufactured by Kabi Co.) is dissolved in a Tris hydrochloric acid buffer solution (pH: 8.3) to prepare a S-2238-0.4 M Tris hydrochloric acid solution having a concentration of 80 m. To 175 l of the solution, an aqueous solution of a compound of the present invention (515 l) is added.
After incubating at 37 C for one minute, 10 l of a bovine thrombin solution (4.4 units/ml, manufactured by Mochida Co., Ltd.) is added. A hydrolysis reaction rate of the substrate is determined by measuring a change in absorbance of 405 nm at 37 C.
The inhibitor concentration exhibiting an absorbance which is half as large as that obtained in case of adding no inhibitor (compound of the present invention) was determined as 150 ( m).
(ii) The measuring method for coagulation inhibition of rat plasma The compound of the present invention is dissolved in water or saline to form a solution of a total volume of 0.1 ml. To the solution, 0.1 ml of rat plasma is added and the mixture is incubated at 37 C for 30 seconds. Then, 0.1 mi of bovine thrombin (8 units/mI, Mochida Co., Ltd.) is added and the coagulation time is measured at 37 C. The concentration of the inhibitor (i.e., the compound of the present invention) which doubles the coagulation time that obtained in the absence of the inhibitor was determined as 150 ( m).
(iii) The measuring method for antithrombin activity of rat plasma on oral administration To a rat abstained from bait overnight, an aqueous solution or suspension of the present compound (inhibitor) (30 mg/kg) is orally administered using an oral sound.
After one hour, 2 ml of blood is collected from cava abdominalis and the antithrombin activity in plasma is measured using a method of the above item (ii). As a control experiment, the coagulation time of blood collected from a rat which has not been administered the inhibitor was measured. The extension effect on the coagulation time is represented by the numerical value obtained by comparing the data with those obtained in control experirnent, wherein the numerical value obtained in the control experiment was assumed to be 1.
Experimental Example 2: Determination of Antitrypsin activity (i) The measuring method for hydrolysis inhibition of synthetic substrate (S-2222) S-2222 (manufactured by Kabi Co.) is dissolved in a'Tris hydrochloric acid (pH: 8.3) to prepare a S-2222-0.4M Tris hydrochloric acid solution having a concentration of 400 m. To the solution (175 l), 515 l of a solution of a compound of the present invention is added. After incubating at 37'C for one minute, 10 l of a bovine trypsin solution (1 to 2 mg/ml, manufactured by Sigma Co.) is added. A hydrolysis reaction rate of the substrate is determined by measuring a change in absorbance of 405 nm at 37 C.
The inhibitor concentration exhibiting an absorbance which is half as large as that obtained in case of adding no inhibitor (compound of the present invention) was determined as 150 ( m).
The results are shown in Table 2.
Tabie 2 Antithrombin activity 150 ( m) Example Synthetic Rat plasma Antitrypsin Thrombiri coagulation time No. substrate method method activity 150 ( m) extensiori coefficient on oral administration 1 0.046 5.97 2 0.030 8.75 3 0.027 4.46 4 0.0076 0.021 0.040 6.70 0.048 6 0.056 3.16 7 0.030 8 0.122 9 0.11 0.17 12 0.083 13 0.72 0.59 0.011 0.038 2.2 16 0.021 1.7 17 0.015 0.053 3.2 18 0.060 19 0.031 0.028 21 0.021 1.0 22 0.014 0.94 23 0.017 0.058 3.6 24 3.28 > 300 2.82 26 4.16 27 3.52 28 4.35 2.75 31 2.77 32 3.58 Antithrombin activity 150 ( m) Example Synthetic Rat plasma Antitrypsin Thrombiri coagulation time No. substrate method method activity 150 ( m) extensiori coefficient on oral administration 33 3.99 35 3.72 36 2.85 37 4.37 39 2.37 40 2.70 41 2.94 42 4.36 43 3.09 46 2.16 47 2.34 48 4.91 49 7.12 50 3.50 51 2.80 52 0.13 0.045 14 4.10 53 0.081 0.059 1.4 54 0.23 56 0.13 0.080 14 2.10 57 0.082 58 0.097 2.35 61 0.056 62 0.088 2.18 64 0.13 1.25 65 3.67 67 0.56 0.081 20 Experimental Example 3: Acute toxicity test Acute toxicity was determined in rat. An approximate lethal dose was determined by conducting an oral acute toxicity test using rits. The results are shown in Table 3.
z14U598 Table 3 Approximate lethal dose mg/kg Male Female Example No.
52 Not less than 2000 Not less thari 2000 33 Not less than 2000 Not less thari 2000 37 Not less than 2000 Not less thari 2000
52 Not less than 2000 Not less thari 2000 33 Not less than 2000 Not less thari 2000 37 Not less than 2000 Not less thari 2000
Claims (11)
1. A prolineamide derivative represented by the formula (I):
wherein:
A is a carbon atom or a nitrogen atom;
n is an integer of 0 to 2;
a broken line is no bond or a single bond;
R1 is wherein:
D and E independently indicate a single bond or an optionally branched C1-C6 alkylene group;
R4 is a C1-C6 alkyl group;
-OR6, R6 is a hydrogen atom, a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted C7-C12 aralkyl group;
-SR7, R7 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted C7-C12 aralkyl group;
-SOR8, R8 is an optionally substituted C6-C10 aryl group or an optionally substituted C3-C8 cycloalkyl group;
-SO2R9, R9 is an optionally substituted C6-C10 aryl group or an optionally substituted C3-C8 cycloalkyl group;
-COR10, R10 is a hydroxyl group, a C1-C6 alkoxy group, an optionally substituted C6-C10 aryl group or an optionally substituted C3-C8 cycloalkyl group;
-NHR11, R11 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted C7-C12 aralkyl group;
-NHCOR12, R12 is a C1-C6 alkoxy group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted C7-C12 aralkyloxy group:
-NHSO2R13, R13 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group, an optionally substituted C7-C12 aralkyl group, or an optionally substituted 5- to 10-membered heterocyclic group;
an optionally substituted C6-C10 aryl group;
an optionally substituted C3-C8 cycloalkyl group;
an optionally substituted 5- to 10-membered heterocyclic group; or -SiR14R15R16, R14, R15, and R16 independently indicate a C1-C6 alkyl group;
R5 is a-OR17, R17 is a hydrogen atom, -SiR22R23R24, R22, R23, and R24 independently indicate a C1-C6 alkyl group, a C1-C6 alkyl group, or an optionally substituted 5- to 10-membered heterocyclic group;
-OCOR18, R18 is a hydrogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group, an amino group, a C1-C6 alkylamino group, a C2-C12 dialkylamino group or a C2-C7 alkenylamino group;
-NHR19, R19 is a hydrogen atom, a C1-C6 alkyl group or an optionally substituted C7-C12 aralkyl group;
-NHCOR20, R20 is a hydrogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, an optionally substituted C3-C8 cycloalkyl group, a C2-C7 carboxyalkyloxy group, a C2-C7 alkenyloxy group, an optionally substituted C6-C10 aryl group, an optionally substituted C6-C10 aryloxy group, a C3-C9 alkoxycarbonylalkoxy group, a C2-C12 dialkylamino group or an optionally substituted C7-C12 aralkyloxy group; or -NHSO2R21, R21 is a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C2-C7 carboxyalkyl group, an optionally substituted C6-C10 aryl group, a C3-C9 alkoxycarbonylalkyl group or an optionally substituted C7-C12 aralkyl group; and m is 0 or 1;
R2 is a hydrogen atom or a C1-C6 alkyl group; and R3 is -NH2 or -C(=NR25)NH2, wherein R25 is a hydrogen atom, or a hydroxyl group;
in the above optionally substituted C6-C10 aryl group, optionally substituted C8 cycloalkyl group, optionally substituted C7-C12 aralkyl group, optionally substituted C7-C12 aralkyloxy group, optionally substituted 5- to 10-membered heterocyclic group, and optionally substituted C6-C10 aryloxy group, the substituent is a group selected from the group consisting of a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a hydroxy group, a carboxyl group, a C2-C7 carboxyalkyl group, a C2-C7 carboxyalkyloxy group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyl group , a C2-C7 alkoxycarbonyloxy group, a C8-C13 aralkyloxycarbonyl group, a C3-C9 alkoxycarboxyalkoxy group, and a halogen atom, the 5- to 10-membered heterocyclic group for R4, R13 and R17 is selected from the group consisting of furan, tetrahydrofuran, pyran, benzofuran, chroman, thiophene, benzothiophene, pyrrole, imidazole, pyrazole, triazole, pyridine, piperidine, pyrazine, piperazine, pyrimidine, indole, benzimidazole, purine, quinoline, phthalzine, quinazoline, cinnoline, oxazole, thiazole, and morpholine, provided that R3 is -C(=NR25)NH2 (R25 is as defined above) when A is a nitrogen atom, and further provided that when R4 and R5 are sulphonylamino, R3 is NH2 or a salt or hydrate thereof.
wherein:
A is a carbon atom or a nitrogen atom;
n is an integer of 0 to 2;
a broken line is no bond or a single bond;
R1 is wherein:
D and E independently indicate a single bond or an optionally branched C1-C6 alkylene group;
R4 is a C1-C6 alkyl group;
-OR6, R6 is a hydrogen atom, a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted C7-C12 aralkyl group;
-SR7, R7 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted C7-C12 aralkyl group;
-SOR8, R8 is an optionally substituted C6-C10 aryl group or an optionally substituted C3-C8 cycloalkyl group;
-SO2R9, R9 is an optionally substituted C6-C10 aryl group or an optionally substituted C3-C8 cycloalkyl group;
-COR10, R10 is a hydroxyl group, a C1-C6 alkoxy group, an optionally substituted C6-C10 aryl group or an optionally substituted C3-C8 cycloalkyl group;
-NHR11, R11 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted C7-C12 aralkyl group;
-NHCOR12, R12 is a C1-C6 alkoxy group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group or an optionally substituted C7-C12 aralkyloxy group:
-NHSO2R13, R13 is a C1-C6 alkyl group, an optionally substituted C6-C10 aryl group, an optionally substituted C3-C8 cycloalkyl group, an optionally substituted C7-C12 aralkyl group, or an optionally substituted 5- to 10-membered heterocyclic group;
an optionally substituted C6-C10 aryl group;
an optionally substituted C3-C8 cycloalkyl group;
an optionally substituted 5- to 10-membered heterocyclic group; or -SiR14R15R16, R14, R15, and R16 independently indicate a C1-C6 alkyl group;
R5 is a-OR17, R17 is a hydrogen atom, -SiR22R23R24, R22, R23, and R24 independently indicate a C1-C6 alkyl group, a C1-C6 alkyl group, or an optionally substituted 5- to 10-membered heterocyclic group;
-OCOR18, R18 is a hydrogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group, an amino group, a C1-C6 alkylamino group, a C2-C12 dialkylamino group or a C2-C7 alkenylamino group;
-NHR19, R19 is a hydrogen atom, a C1-C6 alkyl group or an optionally substituted C7-C12 aralkyl group;
-NHCOR20, R20 is a hydrogen atom, a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, an optionally substituted C3-C8 cycloalkyl group, a C2-C7 carboxyalkyloxy group, a C2-C7 alkenyloxy group, an optionally substituted C6-C10 aryl group, an optionally substituted C6-C10 aryloxy group, a C3-C9 alkoxycarbonylalkoxy group, a C2-C12 dialkylamino group or an optionally substituted C7-C12 aralkyloxy group; or -NHSO2R21, R21 is a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C2-C7 carboxyalkyl group, an optionally substituted C6-C10 aryl group, a C3-C9 alkoxycarbonylalkyl group or an optionally substituted C7-C12 aralkyl group; and m is 0 or 1;
R2 is a hydrogen atom or a C1-C6 alkyl group; and R3 is -NH2 or -C(=NR25)NH2, wherein R25 is a hydrogen atom, or a hydroxyl group;
in the above optionally substituted C6-C10 aryl group, optionally substituted C8 cycloalkyl group, optionally substituted C7-C12 aralkyl group, optionally substituted C7-C12 aralkyloxy group, optionally substituted 5- to 10-membered heterocyclic group, and optionally substituted C6-C10 aryloxy group, the substituent is a group selected from the group consisting of a C1-C6 alkyl group, a C1-C6 haloalkyl group, a C1-C6 alkoxy group, a hydroxy group, a carboxyl group, a C2-C7 carboxyalkyl group, a C2-C7 carboxyalkyloxy group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyl group , a C2-C7 alkoxycarbonyloxy group, a C8-C13 aralkyloxycarbonyl group, a C3-C9 alkoxycarboxyalkoxy group, and a halogen atom, the 5- to 10-membered heterocyclic group for R4, R13 and R17 is selected from the group consisting of furan, tetrahydrofuran, pyran, benzofuran, chroman, thiophene, benzothiophene, pyrrole, imidazole, pyrazole, triazole, pyridine, piperidine, pyrazine, piperazine, pyrimidine, indole, benzimidazole, purine, quinoline, phthalzine, quinazoline, cinnoline, oxazole, thiazole, and morpholine, provided that R3 is -C(=NR25)NH2 (R25 is as defined above) when A is a nitrogen atom, and further provided that when R4 and R5 are sulphonylamino, R3 is NH2 or a salt or hydrate thereof.
2. The compound according to claim 1, wherein the 5- to 10-membered heterocyclic group contains 1 to 4 heteroatoms selected from the group consisting of an oxygen atom, a sulfur atom and a nitrogen atom and the total number of atoms constituting the ring is 5 to 10.
3. The compound according to claim 1, wherein A is a carbon atom.
4. The compound according to claim 1, wherein:
n is 1 or 2;
R1 is -D-(CH)m-E-R4 wherein:
D and E independently indicate a single bond or an optionally branched C1-C6 alkylene group;
R4 is a C1-C6 alkyl group;
-OR6, R6 is a C1-C6 alkyl group; a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group; or a C7-C12 aralkyl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group;
-SR7, R7 is a C1-C6 alkyl group; a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group; or a C7-C12 aralkyl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group;
-COOH;
a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group;
a C3-C8 cycloalkyl group; or -SiR14R15R16, R14, R15, and R16 independently indicate a C1-C6 alkyl group;
R5 is -OH, -OCOR18, R18 is a C1-C6 alkoxy group or a C2-C7 alkenylamino group;
-NH2;
-NHCOR20, R20 is a C1-C6 alkoxy group, a C6-C10 aryloxy group, a C3-C9 alkoxycarbonylalkoxy group, a C2-C12 dialkylamino group or a C7-C12 aralkyloxy group; or -NHSO2R21, R21 is a C1-C6 alkyl group, a C2-C7 carboxyalkyl group, a C6-C10 aryl group, a C3-C9 alkoxycarbonylalkyl group or a C7-C12 aralkyl group; and m is 0 or 1;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2, R25 is a hydrogen atom, or a hydroxyl group.
n is 1 or 2;
R1 is -D-(CH)m-E-R4 wherein:
D and E independently indicate a single bond or an optionally branched C1-C6 alkylene group;
R4 is a C1-C6 alkyl group;
-OR6, R6 is a C1-C6 alkyl group; a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group; or a C7-C12 aralkyl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group;
-SR7, R7 is a C1-C6 alkyl group; a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group; or a C7-C12 aralkyl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group;
-COOH;
a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a C1-C6 alkoxy group, a halogen atom, a hydroxyl group, a carboxyl group, a C2-C7 alkoxycarbonyl group, a C2-C7 carboxyalkyl group, a C2-C7 acyl group, a C2-C7 acyloxy group, a C2-C7 alkoxycarbonyloxy group, a C3-C9 alkoxycarbonylalkoxy group and a benzyloxycarbonyl group;
a C3-C8 cycloalkyl group; or -SiR14R15R16, R14, R15, and R16 independently indicate a C1-C6 alkyl group;
R5 is -OH, -OCOR18, R18 is a C1-C6 alkoxy group or a C2-C7 alkenylamino group;
-NH2;
-NHCOR20, R20 is a C1-C6 alkoxy group, a C6-C10 aryloxy group, a C3-C9 alkoxycarbonylalkoxy group, a C2-C12 dialkylamino group or a C7-C12 aralkyloxy group; or -NHSO2R21, R21 is a C1-C6 alkyl group, a C2-C7 carboxyalkyl group, a C6-C10 aryl group, a C3-C9 alkoxycarbonylalkyl group or a C7-C12 aralkyl group; and m is 0 or 1;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2, R25 is a hydrogen atom, or a hydroxyl group.
5. The compound according to claim 1, wherein:
n is 1;
R1 is wherein:
D and E independently indicate a single bond or an optionally branched C1-C6 alkylene group;
R4 is a C1-C6 alkyl group;
-OR6, R6 is a C6-C10 aryl, which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group or C7-C12 aralkyl group;
-SR7, R7 is a C1-C6 alkyl group;
a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group; or a C3-C6 cycloalkyl group;
R5 is -OH;
NH2;
-NHCOR20, R20 is a C1-C6 alkoxy group or a C7-C12 aralkyloxy group;
or -NHSO2R21, R21 is a C1-C6 alkyl group or a C6-C10 aryl group; and mis1;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2, R25 is a hydrogen atom or a hydroxyl group; or -NH2.
n is 1;
R1 is wherein:
D and E independently indicate a single bond or an optionally branched C1-C6 alkylene group;
R4 is a C1-C6 alkyl group;
-OR6, R6 is a C6-C10 aryl, which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group or C7-C12 aralkyl group;
-SR7, R7 is a C1-C6 alkyl group;
a C6-C10 aryl group which may be substituted with at least one substituent selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group; or a C3-C6 cycloalkyl group;
R5 is -OH;
NH2;
-NHCOR20, R20 is a C1-C6 alkoxy group or a C7-C12 aralkyloxy group;
or -NHSO2R21, R21 is a C1-C6 alkyl group or a C6-C10 aryl group; and mis1;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2, R25 is a hydrogen atom or a hydroxyl group; or -NH2.
6. The compound according to claim 1, wherein:
n is 1;
R1 is wherein:
D is a single bond;
E is a single bond or a C1-C6 alkylene group;
R4 is a C1-C6 alkyl group;
-OR6, R6 is a C6-C10 aryl, which may be substituted with one or more substituents selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group or C7-C12 aralkyl group;
-SR7, R7 is a C1-C6 alkyl group;
a C6-C10 aryl group which may be substituted with one or more substituents selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group; or a C3-C6 cycloalkyl group;
R5 is -NH2;
-NHCOR20, R20 is a C1-C6 alkoxy group or a C7-C12 aralkyloxy group; or -NHSO2R21, R21 is a C1-C6 alkyl group or a C6-C10 aryl group; and m is 1;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2, R25 is a hydrogen atom or a hydroxyl group; or -NH2.
n is 1;
R1 is wherein:
D is a single bond;
E is a single bond or a C1-C6 alkylene group;
R4 is a C1-C6 alkyl group;
-OR6, R6 is a C6-C10 aryl, which may be substituted with one or more substituents selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group or C7-C12 aralkyl group;
-SR7, R7 is a C1-C6 alkyl group;
a C6-C10 aryl group which may be substituted with one or more substituents selected from the group consisting of a C1-C6 alkyl group, a halogen atom, a carboxyl group, a C2-C7 carboxyalkyl group and a benzyloxycarbonyl group; or a C3-C6 cycloalkyl group;
R5 is -NH2;
-NHCOR20, R20 is a C1-C6 alkoxy group or a C7-C12 aralkyloxy group; or -NHSO2R21, R21 is a C1-C6 alkyl group or a C6-C10 aryl group; and m is 1;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2, R25 is a hydrogen atom or a hydroxyl group; or -NH2.
7. The compound according to claim 1, wherein:
A is a carbon atom;
n is 1;
R1 is wherein:
D is a single bond;
E is a single bond or a C1-C3 alkylene group;
R4 is a C3-C6 alkyl group, -OR6, R6 is a C1-C6 alkyl group, a phenyl group, or a C3-C6 cycloalkyl group;
R5 is -OH;
-NHR19, R19 is a hydrogen atom;
-NHCOR20, R20 is a C1-C6 alkoxy group; or -NHSO2R21, R21 is a C1-C3 alkyl group; and m is 1;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2, R25 is a hydrogen atom or a hydroxyl group; or -NH2.
A is a carbon atom;
n is 1;
R1 is wherein:
D is a single bond;
E is a single bond or a C1-C3 alkylene group;
R4 is a C3-C6 alkyl group, -OR6, R6 is a C1-C6 alkyl group, a phenyl group, or a C3-C6 cycloalkyl group;
R5 is -OH;
-NHR19, R19 is a hydrogen atom;
-NHCOR20, R20 is a C1-C6 alkoxy group; or -NHSO2R21, R21 is a C1-C3 alkyl group; and m is 1;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2, R25 is a hydrogen atom or a hydroxyl group; or -NH2.
8. The compound according to claim 1, wherein:
n is 1;
R1 is wherein:
D is a single bond;
E is a single bond or a C1-C6 alkylene group;
R4 is a C1-C6 alkyl group;
R5 is -NHCOR20, R20 is a C1-C6 alkoxy group; and m is 1;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2, R25 is a hydrogen atom or a hydroxyl group.
n is 1;
R1 is wherein:
D is a single bond;
E is a single bond or a C1-C6 alkylene group;
R4 is a C1-C6 alkyl group;
R5 is -NHCOR20, R20 is a C1-C6 alkoxy group; and m is 1;
R2 is a hydrogen atom; and R3 is -C(=NR25)NH2, R25 is a hydrogen atom or a hydroxyl group.
9. Trans-4-[(S)-N-((R)-2-ethoxycarbonylamino-4,4-dimethylpentanoyl) prolyl]aminomethylcyclohexanecarboxamidoxime or a salt or hydrate thereof.
10. A pharmaceutical composition comprising a compound as claimed in any one of claims 1 to 10 and a pharmaceutically acceptable carrier therefor.
11. A protease inhibitor comprising a compound as claimed in any one of claims 1 to 9 as the active ingredient together with a pharmaceutically acceptable carrier therefor.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP773394 | 1994-01-27 | ||
| JP007733/1994 | 1994-01-27 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2140598A1 CA2140598A1 (en) | 1995-07-28 |
| CA2140598C true CA2140598C (en) | 2010-03-09 |
Family
ID=11673914
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002140598A Expired - Lifetime CA2140598C (en) | 1994-01-27 | 1995-01-19 | Prolineamide derivatives |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US5744487A (en) |
| EP (1) | EP0669317B1 (en) |
| KR (1) | KR950032114A (en) |
| CN (1) | CN1066712C (en) |
| AT (1) | ATE223378T1 (en) |
| AU (1) | AU1025795A (en) |
| CA (1) | CA2140598C (en) |
| DE (1) | DE69528005T2 (en) |
| ES (1) | ES2182852T3 (en) |
| FI (1) | FI950309A (en) |
| HU (1) | HUT72062A (en) |
| NO (1) | NO950297L (en) |
| NZ (1) | NZ270395A (en) |
| RU (1) | RU95101048A (en) |
| TW (1) | TW306917B (en) |
| ZA (1) | ZA95631B (en) |
Families Citing this family (62)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5583146A (en) * | 1992-12-02 | 1996-12-10 | Bristol-Myers Squibb Company | Heterocyclic thrombin inhibitors |
| US6984627B1 (en) | 1993-06-03 | 2006-01-10 | Astrazeneca Ab | Peptide derivatives |
| SE9301916D0 (en) * | 1993-06-03 | 1993-06-03 | Ab Astra | NEW PEPTIDES DERIVATIVES |
| US5705487A (en) * | 1994-03-04 | 1998-01-06 | Eli Lilly And Company | Antithrombotic agents |
| US5707966A (en) * | 1994-03-04 | 1998-01-13 | Eli Lilly And Company | Antithrombotic agents |
| IL112795A (en) | 1994-03-04 | 2001-01-28 | Astrazeneca Ab | Peptide derivatives as antithrombic agents their preparation and pharmaceutical compositions containing them |
| US5561146A (en) * | 1994-06-10 | 1996-10-01 | Bristol-Myers Squibb Company | Modified guanidino and amidino thrombin inhibitors |
| DE4421052A1 (en) * | 1994-06-17 | 1995-12-21 | Basf Ag | New thrombin inhibitors, their production and use |
| DE4443390A1 (en) * | 1994-12-06 | 1996-06-13 | Basf Ag | New dipeptidic p-amidinobenzylamides with N-terminal sulfonyl or aminosulfonyl residues |
| EA002767B1 (en) * | 1995-02-10 | 2002-08-29 | Басф Акциенгезельшафт | Thrombin inhibitors |
| TR199700803T1 (en) * | 1995-02-17 | 1998-02-21 | Basf Aktiengesellschaft | Novel dipeptidic amidines as thrombin-inhibitors. |
| US5710130A (en) * | 1995-02-27 | 1998-01-20 | Eli Lilly And Company | Antithrombotic agents |
| US5914319A (en) * | 1995-02-27 | 1999-06-22 | Eli Lilly And Company | Antithrombotic agents |
| CA2176414A1 (en) * | 1995-05-18 | 1996-11-19 | S. David Kimball | Acyl guanidine and amidine prodrugs |
| SA96170106A (en) | 1995-07-06 | 2005-12-03 | أسترا أكتيبولاج | New amino acid derivatives |
| NZ312791A (en) | 1995-07-26 | 1999-07-29 | Mitsubishi Chem Corp | Penicillaminamide derivatives |
| AR005245A1 (en) * | 1995-12-21 | 1999-04-28 | Astrazeneca Ab | THROMBIN INHIBITOR PRODROGES, A PHARMACEUTICAL FORMULATION THAT INCLUDES THEM, THE USE OF SUCH PRODROGES FOR THE MANUFACTURE OF A MEDICINAL PRODUCT AND A PROCEDURE FOR ITS PREPARATION |
| AU1990197A (en) * | 1996-03-12 | 1997-10-01 | Bristol-Myers Squibb Company | Carbamyl guanidine and amidine prodrugs |
| US5811402A (en) * | 1996-03-22 | 1998-09-22 | Eli Lilly And Company | Antithrombotic diamides |
| SE9602263D0 (en) | 1996-06-07 | 1996-06-07 | Astra Ab | New amino acid derivatives |
| US5863929A (en) | 1996-06-25 | 1999-01-26 | Eli Lilly And Company | Anticoagulant agents |
| US6200967B1 (en) | 1996-06-25 | 2001-03-13 | Eli Lilly And Company | Anticoagulant agents |
| SE9602646D0 (en) | 1996-07-04 | 1996-07-04 | Astra Ab | Pharmaceutically useful compounds |
| AR013084A1 (en) | 1997-06-19 | 2000-12-13 | Astrazeneca Ab | USEFUL AMIDINE DERIVATIVES AS THROMBIN INHIBITORS, PHARMACEUTICAL COMPOSITION, USE OF SUCH COMPOUNDS FOR THE PREPARATION OF MEDICINES AND THE PROCESS FOR THE PREPARATION OF THE MENTIONED COMPOUNDS |
| DE69805592T2 (en) * | 1997-11-19 | 2003-01-09 | Mitsubishi Chemical Corp., Tokio/Tokyo | A 1/2 sulfate of ((S) -1 - ((S) -2 - ((Trans-4-aminocyclohexylmethyl) carbamoyl) pyrrolidine-1-carbonyl) -2-iso-propylthio-2-methylpropyl) - carbamidsäurepropylesters |
| SE9704543D0 (en) | 1997-12-05 | 1997-12-05 | Astra Ab | New compounds |
| SE9802939D0 (en) | 1998-09-01 | 1998-09-01 | Astra Ab | New process |
| SE9804313D0 (en) | 1998-12-14 | 1998-12-14 | Astra Ab | New compounds |
| CZ20012529A3 (en) | 1999-01-13 | 2001-11-14 | Astrazeneca Ab | Novel amidinobenzylamide derivative and use thereof as thrombin inhibitor |
| FR2791683A1 (en) * | 1999-03-30 | 2000-10-06 | Synthelabo | N-SULFONYL-DIPEPTIDE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION |
| AR023510A1 (en) | 1999-04-21 | 2002-09-04 | Astrazeneca Ab | A TEAM OF PARTS, PHARMACEUTICAL FORMULATION AND USE OF A THROMBIN INHIBITOR. |
| US6316488B1 (en) * | 1999-06-17 | 2001-11-13 | Merck & Co., Inc. | Antibiotic compound |
| SE0001803D0 (en) | 2000-05-16 | 2000-05-16 | Astrazeneca Ab | New compounds i |
| NZ547626A (en) * | 2000-08-11 | 2007-10-26 | Wilex Ag | Non-covalent inhibitors of urokinase and blood vessel formation |
| ES2285989T3 (en) * | 2000-08-11 | 2007-12-01 | Wilex Ag | NON-COVALENT INHIBITORS OF THE UROQUINASE AND THE FORMATION OF BLOOD VESSELS. |
| US6433186B1 (en) | 2000-08-16 | 2002-08-13 | Astrazeneca Ab | Amidino derivatives and their use as thormbin inhibitors |
| US7129233B2 (en) | 2000-12-01 | 2006-10-31 | Astrazeneca Ab | Mandelic acid derivatives and their use as thrombin inhibitors |
| AR035216A1 (en) * | 2000-12-01 | 2004-05-05 | Astrazeneca Ab | MANDELIC ACID DERIVATIVES, PHARMACEUTICALLY ACCEPTABLE DERIVATIVES, USE OF THESE DERIVATIVES FOR THE MANUFACTURE OF MEDICINES, TREATMENT METHODS, PROCESSES FOR THE PREPARATION OF THESE DERIVATIVES, AND INTERMEDIARY COMPOUNDS |
| JP4179878B2 (en) | 2001-02-02 | 2008-11-12 | 中外製薬株式会社 | Peptide derivatives |
| US7195759B2 (en) * | 2001-06-06 | 2007-03-27 | The University Of Manitoba | Therapeutic uses of glandular kallikrein |
| US20090162342A1 (en) * | 2001-06-07 | 2009-06-25 | Sanomune Inc. | Therapeutic uses of glandular kallikrein |
| AR034517A1 (en) | 2001-06-21 | 2004-02-25 | Astrazeneca Ab | PHARMACEUTICAL FORMULATION |
| DE50310038D1 (en) | 2002-03-11 | 2008-08-07 | Curacyte Ag | INGREDIENTS OF UROKINASE, THEIR PREPARATION AND USE |
| SE0201661D0 (en) | 2002-05-31 | 2002-05-31 | Astrazeneca Ab | New salts |
| SE0201659D0 (en) * | 2002-05-31 | 2002-05-31 | Astrazeneca Ab | Modified release pharmaceutical formulation |
| DE10234058A1 (en) * | 2002-07-26 | 2004-02-05 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | New substituted benzoic acid amides, their production and their use as medicines |
| DE10301300B4 (en) | 2003-01-15 | 2009-07-16 | Curacyte Chemistry Gmbh | Use of acylated 4-amidino- and 4-guanidinobenzylamines for the inhibition of plasma kallikrein |
| US7781424B2 (en) * | 2003-05-27 | 2010-08-24 | Astrazeneca Ab | Modified release pharmaceutical formulation |
| DE10342108A1 (en) * | 2003-09-11 | 2005-04-14 | Curacyte Chemistry Gmbh | Basic substituted benzylamine analogs as coagulation factor Xa inhibitors, their preparation and use |
| US7795205B2 (en) | 2004-04-12 | 2010-09-14 | Canyon Pharmaceuticals, Inc. | Methods for effecting regression of tumor mass and size in a metastasized pancreatic tumor |
| US7524354B2 (en) * | 2005-07-07 | 2009-04-28 | Research Foundation Of State University Of New York | Controlled synthesis of highly monodispersed gold nanoparticles |
| DE102005044319A1 (en) | 2005-09-16 | 2007-03-22 | Curacyte Chemistry Gmbh | 2- (Aminomethyl) -5-chloro-benzylamide derivatives and their use as inhibitors of coagulation factor Xa |
| CN101033209B (en) * | 2006-03-09 | 2014-08-27 | 上海医药工业研究院 | Method of preparing pharmaceutical intermediate of (2S,4R)-4-hydroxy-N,N-dimethyl-2-pyrrolidineformamide |
| DE102006050672A1 (en) | 2006-10-24 | 2008-04-30 | Curacyte Discovery Gmbh | New glycylglycine derivatives with a benzylsulfonylamido group and an amidino-organylamido group at the opposite chain ends, used in drugs for reducing loss of blood, e.g. in operations |
| TW200827336A (en) | 2006-12-06 | 2008-07-01 | Astrazeneca Ab | New crystalline forms |
| US20090061000A1 (en) * | 2007-08-31 | 2009-03-05 | Astrazeneca Ab | Pharmaceutical formulation use 030 |
| CN102464701B (en) * | 2010-11-08 | 2015-10-21 | 上海医药工业研究院 | One class novel cpd, Preparation Method And The Use |
| WO2012083436A1 (en) * | 2010-12-21 | 2012-06-28 | The Medicines Company (Leipzig) Gmbh | Trypsin-like serine protease inhibitors, their preparation and use as selective inhibitors of the clotting factors iia and xa |
| US20130315891A1 (en) | 2012-05-25 | 2013-11-28 | Matthew Charles | Formulations of human tissue kallikrein-1 for parenteral delivery and related methods |
| CA2880085C (en) | 2012-06-04 | 2021-09-07 | Diamedica Inc. | Human tissue kallikrein 1 glycosylation isoforms |
| CA3054962A1 (en) | 2017-03-09 | 2018-09-13 | Rick PAULS | Dosage forms of tissue kallikrein 1 |
| WO2024169765A1 (en) * | 2023-02-16 | 2024-08-22 | 上海华汇拓医药科技有限公司 | Salt of dipeptide compound, preparation method therefor, and use thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0813834B2 (en) * | 1990-08-01 | 1996-02-14 | 日東紡績株式会社 | Tripeptide derivative and proteolytic enzyme inhibitor containing the same as active ingredient |
| CA2075154A1 (en) * | 1991-08-06 | 1993-02-07 | Neelakantan Balasubramanian | Peptide aldehydes as antithrombotic agents |
| EP0627929B1 (en) * | 1992-02-14 | 1998-09-30 | Corvas International, Inc. | Inhibitors of thrombosis |
| AU675981B2 (en) * | 1992-12-02 | 1997-02-27 | Bristol-Myers Squibb Company | Guanidinyl-substituted heterocyclic thrombin inhibitors |
-
1995
- 1995-01-19 CA CA002140598A patent/CA2140598C/en not_active Expired - Lifetime
- 1995-01-19 AU AU10257/95A patent/AU1025795A/en not_active Abandoned
- 1995-01-21 TW TW084100530A patent/TW306917B/zh active
- 1995-01-24 FI FI950309A patent/FI950309A/en unknown
- 1995-01-25 NZ NZ270395A patent/NZ270395A/en not_active IP Right Cessation
- 1995-01-26 NO NO950297A patent/NO950297L/en unknown
- 1995-01-26 ES ES95101059T patent/ES2182852T3/en not_active Expired - Lifetime
- 1995-01-26 US US08/378,615 patent/US5744487A/en not_active Expired - Lifetime
- 1995-01-26 AT AT95101059T patent/ATE223378T1/en not_active IP Right Cessation
- 1995-01-26 ZA ZA95631A patent/ZA95631B/en unknown
- 1995-01-26 RU RU95101048/04A patent/RU95101048A/en unknown
- 1995-01-26 HU HU9500240A patent/HUT72062A/en unknown
- 1995-01-26 EP EP95101059A patent/EP0669317B1/en not_active Expired - Lifetime
- 1995-01-26 DE DE69528005T patent/DE69528005T2/en not_active Expired - Lifetime
- 1995-01-27 KR KR1019950001519A patent/KR950032114A/en not_active Application Discontinuation
- 1995-01-27 CN CN95100042A patent/CN1066712C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| RU95101048A (en) | 1996-10-27 |
| NO950297D0 (en) | 1995-01-26 |
| DE69528005D1 (en) | 2002-10-10 |
| EP0669317A1 (en) | 1995-08-30 |
| HUT72062A (en) | 1996-03-28 |
| CA2140598A1 (en) | 1995-07-28 |
| KR950032114A (en) | 1995-12-20 |
| TW306917B (en) | 1997-06-01 |
| EP0669317B1 (en) | 2002-09-04 |
| NO950297L (en) | 1995-07-28 |
| DE69528005T2 (en) | 2003-04-17 |
| ZA95631B (en) | 1995-10-05 |
| ATE223378T1 (en) | 2002-09-15 |
| US5744487A (en) | 1998-04-28 |
| AU1025795A (en) | 1995-08-03 |
| CN1066712C (en) | 2001-06-06 |
| FI950309A (en) | 1995-07-28 |
| ES2182852T3 (en) | 2003-03-16 |
| NZ270395A (en) | 1997-06-24 |
| FI950309A0 (en) | 1995-01-24 |
| CN1121068A (en) | 1996-04-24 |
| HU9500240D0 (en) | 1995-03-28 |
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